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Effects of Rimonabant on Walking Abilities in Incomplete Spinal Cord Injury — RIMOFATSCI-1  

Spinal Cord Injuries Clinical Trial

Official title:
Effects of Rimonabant on Walking Abilities in Incomplete Spinal Cord Injury: a Proof-of-concept Study

Clinical Trial Summary

Randomized placebo-controlled safety and feasibility study with crossover design (3 arms). Placebo or Rimonabant 2.5mg or Rimonabant 5mg will be administered for 5 days. Exploratory efficacy will be tested using six-min walking test.

Clinical Trial Description

Randomized placebo-controlled safety and feasibility study with crossover design (3 arms). Placebo or Rimonabant 2.5mg or Rimonabant 5mg will be administered for 5 days. Exploratory efficacy will be tested using six-min walking test. Main goal is to test safety of Rimonabant in a specific population (incomplete spinal cord injury). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05398913
Study type Interventional
Source Hospital Nacional de Parapléjicos de Toledo
Contact
Status Completed
Phase Phase 1/Phase 2
Start date May 12, 2021
Completion date June 7, 2022
View Details
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