跳至主要内容
临床试验/NCT06231212
NCT06231212已完成2 期

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

Chulalongkorn University1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2020年8月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
23
试验地点
1
主要终点
Efficacy of ECa 233 for pain intensity

研究概览

简要总结

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.

详细描述

ECa 233 is a standardized extract of Centella asiatica with known anti-inflammatory properties and an acceptable safety profile. Hence, it would be relevant to evaluate the anti-inflammatory and pain reducing effects of ECa 233 on subjects with acute TMD, as well as jaw functional movements. A randomized, double-blind, placebo- and active-controlled clinical trial was performed on 18 to 50-year-old participants with acute TMD. These were randomly assigned to four treatment groups for 14 days: placebo, ibuprofen, ECa 233 250mg and 500 mg. At baseline, subjects reported 5 to 8 of pain intensity on a numerical rating scale (NRS). No medications were self-reported 24 h before and during the trial and no systemic conditions were diagnosed. Degenerative joint disease was screened before treatment. Pain intensity levels, mandibular range of motion including pain-free, unassisted and assisted mouth opening at baseline and days7 and 14 post-treatment. Masticatory muscle and jaw joint tenderness were evaluated upon palpation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

ECa groups

Experimental

Intervention group takes capsules containing of ECa 233, an active substance composed of Madecassoside and Asiaticoside

干预措施: ECa 233 (Drug)

NSAID group

Active Comparator

Active-controlled group was given capsules containing 200 mg of ibuprofen

干预措施: Ibuprofen (Drug)

Placebo group

Placebo Comparator

Placebo-controlled group received capsules containing 250 mg of lactose

干预措施: Placebo (Other)

结局指标

主要结局

Efficacy of ECa 233 for pain intensity

时间窗: 14 days

The pain intensity self-reported levels and other clinical parameters were collected at 3 time points: pre-intervention (baseline), 7 and 14 days post-intervention. The pain intensity score was determined by using a 10-point ordinal scale (0 representing no pain and 10 indicating severe pain).

Efficacy of ECa 233 capsules for jaw function

时间窗: 14 days

Mandibular range of motion, including pain-free, unassisted and assisted mouth opening,

Clinical efficacy of ECa 233 capsules in reducing areas of pain on palpation

时间窗: 14 days

The number of masticatory muscles and TMJs with pain upon palpation were counted on the left and right sides. The total score ranged from 0-12 locations

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prangtip Potewiratnanond D.D.S, M.Sc., Ph.D.

Dr.

Chulalongkorn University

研究点 (1)

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