drugset / Trial / NCT03899584

High Doses of 4-aminopyridine in Clinically Complete Chronic Spinal Cord Injury Patients.

NCT03899584

RandomizedParallel-groupDouble-blindTreatment

Summary

150 patients with clinically complete chronic spinal cord Injury will be included in a randomized, parallel, placebo controlled, multi-centric, phase III trial. Patients will be evaluated before starting the medication, and at the end of the treatment in the locomotor, sensory, grade of independence, sensitivity and control of bladder and anal sphincters, quality of life, and psychogenic erection in males. Patients will be divided randomly into two groups where one will receive placebo and the other one 4-Aminopyridine (4-AP) in a maximum of 30 weeks in increasing doses.

Timeline

Start
2019-07-17
Primary completion
2022-12
Completion
2023-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dalfampridine Small molecule 1 mg/kg Oral

Indications