Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04335968
Other study ID # P180594
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date January 23, 2021
Est. completion date April 30, 2024

Study information

Verified date May 2023
Source Assistance Publique - Hôpitaux de Paris
Contact Stéphanie Sigaut
Phone 1 40 87 59 11
Email stephanie.sigaut@aphp.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Postoperative delirium (POD) is one of the most frequent complications after surgery in elderly patients, affecting between 20 and 40% of patients older than 60 after major surgery. This complication has huge consequences for the patients, families and society: increase of morbidity and mortality, prolonged length of stay, cognitive and functional decline leading to loss of autonomy, and important additional healthcare costs. Among numerous risk factors identified, perioperative inflammatory stress is a key element in delirium genesis: surgical trauma releases danger signals in systemic circulation, activating immune cells and leading to neuroinflammation. Melatonin is a neurohormone regulating circadian rhythm. But it also exhibits antioxidant and free radical scavenger properties, and regulates energy metabolism and immune function. It has already demonstrated a neuroprotective potential in various animal models. Its use against delirium is promising: it decreases delirium incidence in elderly patients hospitalized in medical ward, and several studies are now recruiting in ICU. The hypothesis of the trial is that in a high-risk population, perioperative melatonin can reduce the incidence of POD. The main objective is to evaluate the effect of perioperative melatonin administration on postoperative delirium incidence in the first 10 days after surgery, in elderly patients (over 70 years old) being hospitalized and scheduled for acute surgery of fractured lower limb (from femoral head to tibial plateau). This is a prospective, national multicentric (24 centers), phase III, superiority, comparative randomized (1:1) double-blinded clinical trial with two parallel arms: Experimental group: melatonin 4mg per os every night, starting the evening before surgery (or 2 hours before emergency surgery) and until day 5 after surgery. Control group: placebo of this drug with the same schedule, during the same period of time. The patients are aged 70 or older, hospitalized and scheduled for surgery of a severe fracture of a lower limb (from femoral head to tibial plateau).


Description:

Postoperative delirium (POD) is one of the most frequent complications after surgery in elderly patients, affecting between 20 and 40% of patients older than 60 after major surgery. This complication has huge consequences for the patients, families and society: increase of morbidity and mortality, prolonged length of stay, cognitive and functional decline leading to loss of autonomy, and important additional healthcare costs. Among numerous risk factors identified, perioperative inflammatory stress is a key element in delirium genesis: surgical trauma releases danger signals in systemic circulation, activating immune cells and leading to neuroinflammation. In the brain, especially in hippocampus, proinflammatory cytokines, immune cells recruitment and microglial activation alter synaptic plasticity and lead to acute cognitive dysfunction. Moreover, with aging, an increase in initial neuroinflammatory response and a decrease in subsequent resolution phase are observed. Melatonin is a neurohormone regulating circadian rhythm. But it also exhibits antioxidant and free radical scavenger properties, and regulates energy metabolism and immune function. It has already demonstrated a neuroprotective potential in various animal models. Its use against delirium is promising: it decreases delirium incidence in elderly patients hospitalized in medical ward, and several studies are now recruiting in ICU. Concerning the perioperative period, only two studies with conflicting results are available. The first one (Sultan, 2010), that has shown that melatonin decreases POD incidence, has strong methodological limitations (no calculated sample size, only 53 patients in melatonin group, all patients, even in the control group received melatonin if they developed POD, etc). In the second one (deJonghe, 2014), melatonin had no effect on POD incidence, but showed a reduction in the proportion of patients with POD exceeding 2 days. These conflicting results emphasize the need for a third RCT, with optimized methodology. The hypothesis of the trial is that in a high-risk population, perioperative melatonin can reduce the incidence of POD. The main objective is to evaluate the effect of perioperative melatonin administration on postoperative delirium incidence in the first 10 days after surgery, in elderly patients (over 70 years old) being hospitalized and scheduled for acute surgery of fractured lower limb (from femoral head to tibial plateau). This is a prospective, national multicentric (24 centers), phase III, superiority, comparative randomized (1:1) double-blinded clinical trial with two parallel arms: Experimental group: melatonin 4mg per os every night, starting the evening before surgery (or 2 hours before emergency surgery) and until day 5 after surgery. Control group: placebo of this drug with the same schedule, during the same period of time. The patients are aged 70 or older, hospitalized and scheduled for surgery of a severe fracture of a lower limb (from femoral head to tibial plateau). An ancillary study is also planned in this study with the hypothesise that : - Patients presenting post-operative delirium may exhibit significant perturbations of phenotypic and transcriptomic features of circulating leukocytes, of plasma levels of cytokines, and of oxidative stress level. - Administration of melatonin may prevent these perturbations. Ancillary study concerns Beaujon, Bichat and la Pitié centers.


Recruitment information / eligibility

Status Recruiting
Enrollment 790
Est. completion date April 30, 2024
Est. primary completion date January 31, 2024
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria: - Demographic criteria: patient 70 years old or older - Diagnostic criteria: isolated fracture of a lower limb - Proximal femoral fractures: head, cervical, or trochanteric fractures - Periprosthetic hip fracture - Femoral shaft fracture - Distal femoral fractures: supracondylar or condylar - Periprosthetic knee fracture - Tibial plateau fracture - Treatments/strategies/procedures: scheduled orthopedic surgery (osteosynthesis or arthroplasty) - proxy or care giver knowing baseline cognitive status of the patient present or reachable by phone for an interview Exclusion Criteria: - Patient already taking Melatonin - Contraindications and precaution for use of Melatonin administration: - Hypersensitivity to the active substance or to any of the excipients of Circadin© - Liver failure (presence of some of the following clinical and biological symptoms: icterus, asterixis, ascites, known esophageal varices, total bilirubin >20 micromol/L, FV <70%), - Cirrhosis (known histological liver fibrosis) - Renal failure with clearance <30 ml/min O Autoimmune disease O Hereditary galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption syndrome - Patients taking fluvoxamine, 5- or 8-methoxypsoralen, cimetidine, oestrogenotherapy, quinolones, carbamazepine, rifampicin - Other concomitant trauma than lower limb fracture(s) - Surgery scheduled in more than 5 days - Patient under mechanical ventilation - Patient refusing to participate - Patient not talking / understanding French (delirium assessment impossible) - Patient already participating to another interventional study - No signed informed consent, - No affiliation to a social security regime Secondary Exclusion Criteria: Secondary exclusion (before randomization): diagnosis of delirium at the CAM assessment at inclusion, or creatinin clearance <30 ml / min and /or biological signs of hepatocellular insufficiency (bilirubin> 20 umol/l and factor V <70%) if samples not available during the anesthesiologist consultation and so performed after inclusion.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Melatonin 4 mg
melatonin 4mg per os every night, starting the evening before surgery (or 2 hours before emergency surgery) and until day 5 after surgery.
Placebo oral tablet
placebo of this drug with the same schedule, during the same period of time.

Locations

Country Name City State
France hôpital Beaujon Clichy-sous-Bois

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative delirium incidence The Confusion Assessment Method (CAM) score, for patients hospitalized in surgery, or CAM-ICU score, for patients hospitalized in ICU will be applied daily during the first 10 days after surgery or end of hospital stay if shorter 10 days after surgery
Secondary Number of days CAM positive CAM will be applied daily during the first 10 days. the minimum 0 and maximum 4 values, and higher scores mean a worse outcome. 10 days after surgery
Secondary Incidence of postoperative sedative or antipsychotic drugs administration from Daily review of the medical chart and prescriptions looking for any sedative or antipsychotic drug administration 10 days after surgery
Secondary Incidence of postoperative physical restrain prescription Daily review of the medical chart and prescriptions looking for physical restraint prescription. 10 days after surgery
Secondary Incidence of postoperative falls Daily review of the medical chart and prescriptions looking for falls, whichever the gravity 10 days after surgery
Secondary Mini Mental State Examination Cognitive testing interview at bedside using the widely used French validated translation of the Mini Mental State Examination.
the minimum 0 and maximum 30 values, and higher scores mean a better outcome.
10 days (or end of hospital stay if shorter)
Secondary Duration of hospital stay Daily review of the medical file 30 days after surgery
Secondary 30 days postoperative mortality Phone call (or visit for those who had not left the hospital) to the patient or caregivers 30 days after surgery
Secondary 30 days postoperative patient autonomy Phone call (or visit for those who had not left the hospital) to the patient or caregivers and evaluation by the Katz Index of activities of daily living.
The minimum and maximum values are respectively 0 and 6, and higher scores mean a better outcome.
30 days after surgery
Secondary 30 days postoperative Quality of life evaluated by EQ5D5L (standardized instrument for measuring generic health status : MOBILITY, SELF-CARE, USUAL ACTIVITIES, PAIN/DISCOMFORT and ANXIETY/ DEPRESSION),) Questionnaire. the minimum 5 and maximum 125 values, and higher scores mean a better outcome. 30 days after surgery
Secondary 30 days postoperative QALYs (quality-adjusted life year) QALYs (quality-adjusted life year) are the utility weights for the 30 day period x30/365. the minimum and maximum values are respectively 0 and1, and higher scores mean a better outcome. 30 days after surgery
Secondary Total hospital costs at 30 days calculated as the cumulative costs of all admissions (in- and outpatient, home care, rehabilitation) over a 30 day period 30 days after surgery
Secondary Incremental cost effectiveness The incremental cost effectiveness ratio is the difference in total costs divided by the difference in the incidence rate of delirium between the two arms 30 days after surgery
Secondary cost utility ratios the incremental cost utility ratio is the difference in total costs divided by the difference in QALYs (quality-adjusted life year) 30 days after surgery
Secondary Occurrence of side effects During the follow-up, daily interview of the patient and review of the medical chart will be performed, looking for side effects of melatonin. 30 days after surgery
See also
  Status Clinical Trial Phase
Completed NCT03657368 - Ventilation Strategy During General Anesthesia for Orthopedic Surgery N/A
Withdrawn NCT02771041 - Assessment of the Influence of Early Preoperative Consultation on Satisfaction and the Average Length of Stay of Patients Who Underwent Total Hip Arthroplasty N/A
Completed NCT02278627 - Impact of a Technique of Massage During the First Week of Hospitalization on the Recycling of the Mobility of the Knee Further to the Installation of Knee Replacement N/A
Recruiting NCT01205295 - Patient Anxiety and Concern as Predictors for the Perceived Quality and Efficacy of Treatment N/A
Completed NCT01389011 - Perfusion Index (PI) and Pleth Variability Index (PVI) in Patients With Interscalene Blocks in Orthopedic Surgery N/A
Completed NCT01063543 - Pharmacokinetics of Fondaparinux in Patients With Major Orthopedic Surgery N/A
Active, not recruiting NCT03629262 - Dexmedetomidine Supplemented Intravenous Analgesia in Elderly After Orthopedic Surgery Phase 4
Not yet recruiting NCT05537155 - Buccal Acupuncture for Delirium Treatment in Older Patients Recovering From Orthopedic Surgery N/A
Completed NCT03532256 - Post-op Crowd Sourcing Health Data Via Text-messaging
Active, not recruiting NCT03366805 - A Patient Education Video Program for Post-Operative Recovery After Upper Extremity Surgery N/A
Completed NCT03769077 - Cycle to Fun - 'Exergames' for Inpatient Rehabilitation for Children/Youth With CP N/A
Recruiting NCT05401058 - Low-dose Droperidol for Prevention of Postoperative Delirium in Elderly Patients After Non-cardiac Surgery N/A
Completed NCT00293631 - Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After Bunionectomy Phase 2
Completed NCT05110690 - Behavioral Activation and Medication Optimization for Perioperative Mental Health Feasibility Study N/A
Completed NCT05120739 - Efficacy of CHX Cloths Versus CHX Soaps for Bathes Before Orthopedic Surgery N/A
Completed NCT00702416 - Ultrasound Guidance for Interscalene Brachial Plexus Block Phase 4
Completed NCT00724035 - Ultrasound-Guided Axillary or Infraclavicular Nerve Block for Upper Limb Surgery Phase 4
Completed NCT00192894 - New Methods to Detect a Decrease in Heart Function Phase 4
Completed NCT05424211 - The Effect of Music Therapy on Pain Level and Analgesic Consumption N/A
Withdrawn NCT00269971 - A Study to Determine an Effective Dose of Epoetin Alfa to Decrease the Number of Units of Blood Required to be Transfused During Hip Replacement Surgery. Phase 3