drugset / Trial / NCT04239469

Phase II Clinical Trial, Use of KL16-012 in Women With Fibromyalgia Refractary to Conventional Treatment.

NCT04239469 ↗

Phase 2 Unknown 44 enrolled Knop Laboratorios
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A double blind randomized placebo controlled trial in 44 women with fibromyalgia and persistent symptoms in spite of use of conventional pharmacotherapy, will be performed in the city of Valparaiso. Patients will be randomized to either placebo or active principle and be followed for 3 months. Assesment of efficacy and safety will be done by measurement of changes in their Fibromyalgia Impact Questionnaire (FIQ) score, Insomnia Severity Index (ISI) score, pain Visual Analogue Scale (VAS) score, plasma cytokine levels and detection of adverse effects. The active principle will be a standardized extract of cannabis sativa containing 1 milligram of tetrahydrocannabinol (THC) and 0.45 milligrams cannabidiol (CBD) per drop.

Timeline

Start
2020-01-15
Primary completion
2020-06-15
Completion
2020-09-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator KL16-012 Unknown 15 unknown Subcutaneous

Indications