drugset / Trial / NCT06231212
Efficacy of a Standardized Centella Asiatica Extract in Patients With Temporomandibular Disorder
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ECa233 | Unknown | 250 mg | Oral |
| Subject | ECa233 | Unknown | 500 mg | Oral |
| Comparator | Ibuprofen | Small molecule | 200 mg | — |