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临床试验/CTRI/2026/03/107143
CTRI/2026/03/107143尚未招募不适用

Assessment of pain relief and functional improvement following intra articular nanofat grafting in adults with temporomandibular joint internal derangement: A prospective interventional study.

Muhammed Jaseel S V1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2026年6月10日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
17
试验地点
1

研究概览

简要总结

Temporomandibular disorders (TMD-ID) are a common cause of chronic orofacial pain and functional limitation affecting mastication and quality of life. Persistent symptoms despite conservative management necessitate evaluation of alternative therapeutic modalities.

This single-arm interventional study aims to evaluate the efficacy of intra-articular nanofat graft injection in patients clinically diagnosed with temporomandibular disorder internal derangement (TMD-ID) based on the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) Axis I.

The primary objective of the study is to assess the effectiveness of intra-articular nanofat graft injection in reducing pain and improving mandibular function in patients with TMD-ID.

A total of 9 participants (17 temporomandibular joints) will be included in the study. Following baseline clinical assessment, eligible patients will receive intra-articular nanofat graft injection under aseptic conditions.

Participants will be followed up at 1 week, 1 month, and 3 months post-procedure. At each visit, pain intensity, maximum mouth opening, mandibular movements, and functional limitation will be assessed. The total duration of follow-up for each participant will be 3 months.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients aged between 18–50 years -Patients with ASA class 1 and 2 physical status -Patients clinically diagnosed with disc displacement with reduction or disc displacement without reduction according to DC/TMD Axis I diagnostic criteria.
  • Patients who are refractory to conservative management for more than a period of 3 months.

排除标准

  • Local infection at donor or recipient site -Lactating or pregnant women -Previous Temporomandibular joint surgery or intra-articular injections within 6 months -Systemic steroid or immunosuppressive therapy.

研究者

发起方
Muhammed Jaseel S V
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Muhammed Jaseel S V

Yenepoya Dental College

研究点 (1)

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