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Afibrinogenemia clinical trials

View clinical trials related to Afibrinogenemia.

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NCT ID: NCT05360186 Recruiting - Clinical trials for First Trimester Abortion

New Cross-linked Hyaluronan Gel to Prevent Adhesion After USG-MVA: RCT

Start date: June 14, 2022
Phase: N/A
Study type: Interventional

The objective of this prospective, randomized controlled study was to evaluate the effectiveness of this NCH gel in the prevention of IUA development as assessed by hysteroscopy after USG-MVA, in the treatment for first-trimester miscarriage. - To study the severity and extent of the IUA as assessed by the AFS and ESGE adhesion score in both groups of patients. - To examine the rate of complications or side effects with the NCH gel. - To assess the subsequent menstrual history and reproductive outcome in both groups of patients.

NCT ID: NCT05072912 Terminated - Clinical trials for Previous Diagnosis With a Complement-mediated Disease and/or With Clinical Manifestations Reasonably Associated With Complement Factor I Deficiency

Screening Study to Identify Patients With Complement Factor I Deficiencies

Start date: July 21, 2021
Phase:
Study type: Observational

This is screening study to identify patients with Complement Factor I deficiencies. The primary objective is to identify participants with CFI deficiencies and assess the prevalence in the screened population.

NCT ID: NCT04636268 Withdrawn - Hypofibrinogenemia Clinical Trials

FIB Grifols Congenital Deficiency for On-demand Treatment and Surgical Prophylaxis

Start date: December 2023
Phase: Phase 3
Study type: Interventional

This is a phase 3, multi-center, prospective, open-label, single-arm, clinical trial to be carried out in subjects with congenital fibrinogen deficiency manifested as afibrinogenemia or severe hypofibrinogenemia. This clinical trial is planned to be performed at study sites in multiple countries. It is planned to include a maximum of 32 adult and pediatric subjects with congenital fibrinogen deficiency in order to provide at least 28 evaluable acute bleeding episodes and/or surgical procedures.

NCT ID: NCT03920332 Completed - Clinical trials for Afibrinogenemia, Congenital

Pregnancy and Fibrinogen Disorders

FIBRINOGEST
Start date: September 1, 2019
Phase:
Study type: Observational

The aim of this observational study is to evaluate the prevalence of uncomplicated pregnancies in women suffering from congenital fibrinogen disorders (i.e, hypofibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia) as well as to describe pregnancies outcomes in such diseases.

NCT ID: NCT03793426 Recruiting - Clinical trials for Congenital Fibrinogen Deficiency

Safety and Efficacy of Fibryga in Congenital Fibrinogen Deficiency

Start date: January 28, 2021
Phase:
Study type: Observational

Open-label, Uncontrolled, Multicenter Observational Study on the Safety and Efficacy of Fibryga in Congenital Fibrinogen Deficiency

NCT ID: NCT03484065 Completed - Clinical trials for Afibrinogenemia, Congenital

Quality of Life in Patients With Congenital Afibrinogenemia

QualyAFIB
Start date: June 2016
Phase:
Study type: Observational

The aim of this observational study is to evaluate the quality of life in patients with congenital afibrinogenemia using the Haemo-QoL SF for kids and the Haem-A-QoL for adult patients.

NCT ID: NCT02822599 Completed - Hypofibrinogenemia Clinical Trials

Human Fibrinogen Concentrate in Pediatric Cardiac Surgery

RiaSTAP
Start date: June 1, 2017
Phase: Phase 4
Study type: Interventional

The goal of the study is to determine whether the use of Human Fibrinogen Concentrate (RiaSTAP) will decrease blood loss and the need for component blood therapy in neonates and infants undergoing cardiopulmonary bypass.

NCT ID: NCT02427217 Completed - Clinical trials for Congenital Fibrinogen Deficiency

An Observational Cohort Study of the Safety and Efficacy of Fibrinogen Concentrate, Human (FCH) in Subjects With Congenital Fibrinogen Deficiency

Start date: May 7, 2015
Phase: N/A
Study type: Observational

This is a multicenter, non interventional, retrospective cohort study with a prospective, observational follow-up component to investigate the safety and efficacy of FCH use in subjects with congenital fibrinogen deficiency. Data will be collected on the safety and efficacy of FCH as used for the treatment of acute bleeding episodes, routine prophylaxis and perioperative bleeding in these subjects. All subjects have received FCH and may continue to receive FCH at the discretion of the treating physician / Primary Investigator according to the standard of care at the participating study site.

NCT ID: NCT02408484 Completed - Clinical trials for Congenital Fibrinogen Deficiency

Study to Assess the Efficacy, Safety and Pharmacokinetic of Octafibrin in Paediatric Subjects With Fibrinogen Deficiency

Start date: December 2015
Phase: Phase 3
Study type: Interventional

This study will assess the efficacy of Octafibrin, a fibrinogen concentrate in in the on-demand treatment of spontaneous or traumatic bleeding episodes in paediatric patients less than 12 years of age.The planned study duration is up to 5 years. The study will be considered completed when a minimum of 6 subjects (i.e., at least 3 subjects aged between 0 and <6 years and 3 subjects aged between 6 and <12 years) have at least one documented bleeding episode and when in total a minimum of 2 surgical procedures have been performed. All patients will undergo a pharmacokinetic (PK) study after screening. This will have a duration of 14 days, after which a patient can be treated for a bleeding episode or planned surgical procedure when they occur.

NCT ID: NCT02281500 Completed - Clinical trials for Congenital Afibrinogenemia

Pharmacokinetics, Efficacy, and Safety of Human Plasma-Derived Fibrinogen (FIB Grifols) in Participants With Congenital Afibrinogenemia

IG0902
Start date: July 22, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The main objective of this study was to evaluate the pharmacokinetics (PK), efficacy, and safety of human plasma-derived fibrinogen concentrate FIB Grifols after a single-dose 70 milligrams/kilogram (mg/kg) body weight administration.