drugset / Trial / NCT05398913

Effects of Rimonabant on Walking Abilities in Incomplete Spinal Cord Injury

NCT05398913

Phase 1/2 Completed 8 enrolled Hospital Nacional de Parapléjicos de Toledo
RandomizedCrossoverQuadruple-blindTreatment

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.

Timeline

Start
2021-05-12
Primary completion
2022-06-07
Completion
2022-06-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Rimonabant Small molecule 2.5 mg
Comparator Rimonabant Small molecule 5 mg

Indications