Effect of Prophylactic Fibrinogen Concentrate In Scoliosis Surgery

Bleeding Clinical Trial

— EFISS  

Official title:

Effect of Prophylactic Fibrinogen Concentrate In Scoliosis Surgery: A Randomized Pilot Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05391412
• Other study ID #: CT0012022
• Status: Recruiting
• Phase: Phase 4
• Start date: June 6, 2022
• Est. completion date: September 30, 2023

Study information

• Verified date: March 2023
• Source: Brno University Hospital
• Contact: Roman Gal, prof.
• Phone: 532233850
• Email: gal.roman[@]fnbrno.cz
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

EFISS is a prospective, randomized, placebo-controlled trial testing the feasibility, safety and efficacy of prophylactic administration of fibrinogen in paediatric spinal surgery. The study is monocentric and will be conducted in University Hospital Brno, Czech Republic. This is a pilot study in which the primary objective will be to evaluate the feasibility of a clinical trial in 32 selected patients undergoing scoliosis surgery. Participants will be randomized into study groups in a 1:1 allocation ratio and followed up for 28 days after surgery. The expected duration of this clinical trial is 8 months.

Description:

Scoliosis is an abnormal lateral curvature of the spine. It is most commonly diagnosed in childhood and early adolescence. Surgical treatment is indicated for severe scoliosis to reduce back pain, neurological symptoms and prevent deterioration of respiratory and cardiovascular function. Scoliosis surgery is often accompanied by a large blood loss and blood transfusion is necessary in 30% to 60% of operated patients. The limited availability, high cost and risk of complications associated with the administration of transfusion products has led to efforts to introduce procedures that aim to reduce the magnitude of blood loss during surgery. Fibrinogen plays an important role in coagulum formation and bleeding arrest. Insufficient fibrinogen levels lead to impaired blood clotting and increased bleeding during major surgery. It has also been shown that patients with higher preoperative fibrinogen levels have less perioperative blood loss. Prophylactic administration of fibrinogen leads to a reduction in blood loss and the number of transfusions administered in some types of procedures. Prophylactic administration of fibrinogen at a dose of 30 mg/kg has been shown to be safe even in paediatric patients. Whether prophylactic fibrinogen administration before scoliosis surgery has an effect on the magnitude of blood loss is unclear. To plan a sufficiently large randomized trial to clarify the effect of prophylactic fibrinogen administration before elective scoliosis surgery on the magnitude of blood loss, and the need for transfusion administration, our team of investigators decided to organize this pilot study. Prophylactic administration of fibrinogen has been widely described in various indications in recent decades. Among others, it is mainly cardiovascular surgery, where some authors refer the absence of the effect of fibrinogen administration on postoperative bleeding and some even the association with increased allogeneic blood product transfusion. On the contrary, one-hundred sixteen patients undergoing heart surgery with an expected cardiopulmonary bypass were part of the placebo-controlled double-blind study in which fibrinogen concentrate significantly reduced postoperative bleeding with a significant reduction in allogeneic blood products transfusions. Reduction of bleeding after coronary artery bypass graft without signs of postoperative hypercoagulability associated with preoperative infusion of fibrinogen concentrate is descibed. Fibrinogen administration has also been tested in double-blind placebo-controlled clinical trials associated with urologic surgery and gynaecological surgery procedures. Regarding skeletal surgery, the effect of prophylactically administered fibrinogen on postoperative bleeding has also been studied. Intraoperative administration of fibrinogen was successfully used to significantly decrease bleeding and transfusions in 30 children aged 6 months to 17 years undergoing craniosynostosis surgery. Compared to these results, no differences in blood loss and transfusion requirements were found between treated and placebo groups in younger paediatric patients up to 25 months during craniofacial surgery. Clinical trials directly related to spinal surgery have also been described. This clinical study was performed in 30 adult patients undergoing lumbar surgery, in which 1g of fibrinogen dissolved in distilled water was injected near the surgical incision in the intervention group (n=15). Bleeding during and after surgery in the control group was significantly higher than in the intervention group (P<0.05), and therefore the efficacy of fibrinogen was demonstrated in this indication. Efficacy and safety of preoperatively administrated fibrinogen concentrate (30 mg / kg to 2 g maximum) have also been confirmed in the paediatric population. A total of 102 children (12 - 18 years) with idiopathic scoliosis undergoing surgery were randomized to test and control groups (n=51), where fibrinogen infusion reduced median perioperative bleeding by approximately 155 ml compared to placebo. Fibrinogen administrated in the test group in this case did not reduce the amount of allogeneic blood product transfusion. The clinical outcome of an individual participant in the prophylactic administration of fibrinogen prior to scoliosis surgery may or may not be improved. If effective, this administration will reduce blood loss during surgery and reduce the need for blood transfusions. In any case, participation in this study will improve knowledge about the prophylactic use of fibrinogen during scoliosis surgery, and all participants in this study will contribute to this socially beneficial knowledge. The same surgical procedure will be used in both study groups as is standard in the surgical treatment of spinal scoliosis. The method is generally well tolerated by patients and does not pose significant risks. The potential risks of participating in the EFISS study may include the rare development of adverse reactions, including fever, allergic and anaphylactic reactions, or thromboembolic events associated with the administration of investigational medicinal product.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 32
• Est. completion date: September 30, 2023
• Est. primary completion date: July 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 18 Years

Eligibility

Inclusion Criteria:

Subjects will be eligible for the trial if they meet all of the following criteria:

1. Age < 18 years of age at the time of enrolment

2. Elective scoliosis surgery

3. Signed the relevant informed consent form (more in Chapter 10.1)

4. Sexually active participants (= 15 years old) must agree to the use of following

methods of contraception for the duration of this clinical trial:

1. Women - proper use of a highly reliable method of contraception, i.e. combined hormonal contraception (oral, vaginal or transdermal form), gestagen hormonal contraceptives associated with ovulation inhibition (oral or injectable form) or sexual abstinence.

2. Men - sexual abstinence or the use of an adequate contraceptive method (i.e. condom) in case of sexual intercourse. Exclusion Criteria:

Subjects will not be eligible for the trial if they meet any of the following criteria:

1. Diagnosed congenital or acquired coagulopathy

2. Use of anticoagulants with the exception of perioperative prophylactic administration of Low molecular weight heparin (LMWH) to prevent venous thromboembolism (VTE)

3. Known hypersensitivity to the active substance or to any of the excipients of Investigational Medicinal Product (IMP)

4. History of deep vein thrombosis or pulmonary embolism

5. Pregnancy and lactation

Related Conditions & MeSH terms

• Bleeding
• Blood Coagulation Disorders
• Coagulopathy, Consumption
• Disseminated Intravascular Coagulation
• Fibrinogen
• Hemostatic Disorders
• Scoliosis
• Spine Deformity

Intervention

Drug:
• Fibrinogen Concentrate Human
Patients in the intervention group will receive single administration of fibrinogen concentrate intravenously at a dose of 20-30 mg/kg (depending on body weight and clinical condition, according to SmPC). The medicinal product will be diluted in a 100 ml infusion bag and administered after induction of anaesthesia prior beginning of surgery. The infusion rate should not exceed approximately 5 ml per minute.

Locations

Country	Name	City	State
Czechia	University Hospital Brno	Brno

Sponsors (1)

Lead Sponsor	Collaborator
Brno University Hospital

Country where clinical trial is conducted

Czechia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adverse event	The following primary endpoint will be monitored to evaluate the primary objective: Adverse event - Any untoward medical occurrence in a patient or clinical trial subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment.	through study completion, an average of 6 months
Primary	Adverse drug reaction	The following primary endpoint will be monitored to evaluate the primary objective: Adverse drug reaction - All untoward and unintended responses to an investigational medicinal product related to any dose administered	through study completion, an average of 6 months
Primary	Serious adverse event and reaction	The following primary endpoint will be monitored to evaluate the primary objective: Serious adverse event and reaction - A serious adverse event/reaction is any untoward medical occurrence or effect that at any dose: Results in death; Is life-threatening; Requires hospitalization or extension of existing hospitalization; Results in persistent or significant disability or incapacity; Is a congenital anomaly or birth defect	through study completion, an average of 6 months
Primary	Unexpected adverse reaction	The following primary endpoint will be monitored to evaluate the primary objective: Unexpected adverse reaction - Adverse reaction, the nature, severity, or outcome of which	through study completion, an average of 6 months
Primary	Suspected unexpected serious adverse reaction	The following primary endpoint will be monitored to evaluate the primary objective: Suspected unexpected serious adverse reaction - Any suspected adverse reaction related to the study treatment that is both serious and unexpected.	through study completion, an average of 6 months
Secondary	Deep-vein thrombosis	Incidence of adverse events and reactions according to following Adverse Events of Special Interest (AESI); ? Deep-vein thrombosis verified on duplex ultrasound imaging (YES/NO)	through study completion, an average of 6 months
Secondary	Pulmonary embolism	Incidence of adverse events and reactions according to following Adverse Events of Special Interest (AESI); ? Pulmonary embolism confirmed on CT (YES/NO)	through study completion, an average of 6 months
Secondary	Infection or healing disorder	Incidence of adverse events and reactions according to following Adverse Events of Special Interest (AESI); ? Infection or healing disorder requiring re-surgery and / or initiation of antibiotic therapy (YES/NO)	through study completion, an average of 6 months
Secondary	Length of stay	? Length of stay (LOS) - day of admission - day of discharge will be counted as 1 day	through study completion, an average of 6 months
Secondary	ICU length of stay	? ICU length of stay (ICU LOS) - day of admission - day of discharge will be counted as 1 day	through study completion, an average of 6 months
Secondary	28-day mortality	? 28-day mortality (number of patients who are not alive 28 days after randomization)	at day 28 of study
Secondary	Age	Comparison of demographic characteristics between study groups; ? Age (years)	at the start of the study
Secondary	Sex	Comparison of demographic characteristics between study groups; ? Sex (male, female)	at the start of study
Secondary	Weight	Comparison of demographic characteristics between study groups; ? Weight (kilograms)	at the start of study
Secondary	Haemoglobin	Comparison of laboratory values of selected haematological parameters between study groups; ? Haemoglobin (g/l; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Haematocrit groups	Comparison of laboratory values of selected haematological parameters between study; ? Haematocrit (%; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Platelet count	Comparison of laboratory values of selected haematological parameters between study groups; ? Platelet count (n/l; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Fibrinogen	Comparison of laboratory values of selected haematological parameters between study groups; ? Fibrinogen (g/l; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Activated parcial thromboplastin time (aPTT)	Comparison of laboratory values of selected haematological parameters between study groups; ? aPTT (s; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Prothrombin time (PT)	Comparison of laboratory values of selected haematological parameters between study groups; ? PT (s; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Thrombin time (TT)	Comparison of laboratory values of selected haematological parameters between study groups; ? TT (s; before, at the end of surgery and 24 hours after surgery)	before surgery, immediately after surgery and 24 hours after surgery
Secondary	Total volume of blood loss	Comparison of blood loss level and its compensation between study groups; ? Total volume of blood loss (ml; during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Number of the surgical segments of the spine	Comparison of blood loss level and its compensation between study groups; ? Number of the surgical segments of the spine (n; postoperatively)	immediately after surgery
Secondary	Volume of blood loss for the surgical segment of the spine	Comparison of blood loss level and its compensation between study groups; ? Volume of blood loss for the surgical segment of the spine (ml; during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Urinary output	Comparison of blood loss level and its compensation between study groups; ? Urinary output (ml; in the 24-hour postoperative period)	within the 24-hour postoperative period
Secondary	Red blood cells (RBC) consumption - transfusion unit	Comparison of blood loss level and its compensation between study groups; ? Red blood cells (RBC) consumption (transfusion units consumption during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Red blood cells (RBC) consumption - volume	Comparison of blood loss level and its compensation between study groups; ? Red blood cells (RBC) consumption (total volume of infusion during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Thrombocytes of apheresis (TAD) consumption - transfusion unit	Comparison of blood loss level and its compensation between study groups; ? Thrombocytes of apheresis (TAD) consumption (transfusion units consumption during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Thrombocytes of apheresis (TAD) consumption - volume	Comparison of blood loss level and its compensation between study groups; ? Thrombocytes of apheresis (TAD) consumption (total volume of infusion during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Fresh frozen plasma (FFP) consumption - transfusion unit	Comparison of blood loss level and its compensation between study groups; ? Fresh frozen plasma (FFP) consumption (transfusion units consumption during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Fresh frozen plasma (FFP) consumption - volume	Comparison of blood loss level and its compensation between study groups; ? TFresh frozen plasma (FFP) consumption (total volume of infusion during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Fibrinogen concentrate consumption	Comparison of blood loss level and its compensation between study groups; ? Fibrinogen concentrate consumption (consumption in grams during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Prothrombin complex concentrate (PCC) consumption	Comparison of blood loss level and its compensation between study groups; ? Prothrombin complex concentrate (PCC) consumption (consumption in units during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Blood derivative corresponding to Fresh frozen plasma (Octaplas) consumption	Comparison of blood loss level and its compensation between study groups; ? Blood derivative corresponding to Fresh frozen plasma (Octaplas) consumption (consumption in units during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Crystalloid solutions consumption	Comparison of blood loss level and its compensation between study groups; ? Crystalloid solutions consumption (total volume of infusion during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Colloid solutions consumption	Comparison of blood loss level and its compensation between study groups; ? Colloid solutions consumption (total volume of infusion during surgery and in the 24-hour postoperative period)	during surgery and within the 24-hour postoperative period
Secondary	Number of patients receiving transfusion products	Comparison of blood loss level and its compensation between study groups; ? Number of patients receiving transfusion products	at hospital discharge
Secondary	Number of patients receiving blood derivatives	Comparison of blood loss level and its compensation between study groups; ? Number of patients receiving blood derivatives	at hospital discharge
Secondary	Rate of recruitment of eligible patients who were approached for consent to participate	Feasibility assessment; ? Rate of recruitment of eligible patients who were approached for consent to participate (%; feasibility criterion >75% enrolled participants)	through study completion, an average of 6 months
Secondary	Percentage of missing outcome and clinical data	Feasibility assessment; ? Percentage of missing outcome and clinical data (< 10% missing outcome data including ICU and hospital length of stay (LOS) and survival; < 10% missing clinical data obtained from clinical medical notes and electronic patient records)	through study completion, an average of 6 months