Last updated: May 24, 2023
Sponsor: Assistance Publique - Hôpitaux de Paris
Overall Status: Active - Recruiting
Phase
3
Condition
Orthopedic Surgery
Dementia
Orthopedics
Treatment
Melatonin 4 mg
Placebo oral tablet
Clinical Study ID
NCT04335968
P180594
Ages > 70 All Genders
Study Summary
Eligibility Criteria
Inclusion
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 orarthroplasty)
- proxy or care giver knowing baseline cognitive status of the patient present orreachable by phone for an interview
Exclusion
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 biologicalsymptoms: 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 Hereditarygalactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorptionsyndrome
- 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 atinclusion, or creatinin clearance <30 ml / min and /or biological signs of hepatocellularinsufficiency (bilirubin> 20 umol/l and factor V <70%) if samples not available during theanesthesiologist consultation and so performed after inclusion.
Study Design
Total Participants: 790
Treatment Group(s): 2
Primary Treatment: Melatonin 4 mg
Phase: 3
Study Start date:
January 23, 2021
Estimated Completion Date:
April 30, 2024
Study Description
Connect with a study center
hôpital Beaujon
Clichy-sous-Bois, 93390
FranceActive - Recruiting
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