drugset / Trial / NCT06231212

Efficacy of a Standardized Centella Asiatica Extract in Patients With Temporomandibular Disorder

NCT06231212

Phase 2/3 Completed 23 enrolled Chulalongkorn University
RandomizedSingle-groupTriple-blindTreatment

Summary

The goal of this clinical trial is to test analgesic effect of ECa 233 in subjects with TMD. The main questions it aims to answer are: * Can ECa 233 reduce pain intensity score in subjects with acute TMD? * Can ECa 233 increase jaw functional movements in subjects with acute TMD? Participants will be separated into four groups, including placebo, ibuprofen, low-dosed Eca and high-dosed Eca groups.

Timeline

Start
2020-08-05
Primary completion
2021-09-01
Completion
2022-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ECa233 Unknown 250 mg Oral
Subject ECa233 Unknown 500 mg Oral
Comparator Ibuprofen Small molecule 200 mg