drugset / Trial / NCT07151378

Intestinal Levodopa + Entacapone Therapy (Lecigon®) to Counteract Dopaminergic Desensitization and Neuropsychiatric Complications in Parkinson's Disease

NCT07151378 ↗

Phase 3 Recruiting 150 enrolled University Hospital Tuebingen
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a Phase III multicentric randomized controlled trial with parallel group design and waiting list in patients that have an indication to undergo intestinal L-Dopa + entacapone (Lecigon®) under the existing indication criteria (according to SmPC (Fachinformation) Lecigon®). As primary endpoint, we will analyze the difference of the pre-interventional baseline and 6-month follow-up on the "hyperdopaminergic symptoms" corresponding to section 3 of the "Ardouin Behavioural Scale" hypothesizing on the superiority of LECIG therapy compared to best medical treatment.

Timeline

Start
2025-10-27
Primary completion
2030-09-22
Completion
2030-09-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject LECIG Unknown — —

Indications