Evaluation of clinical efficacy of a new mouth-exercising device in association with local ointment application, intra-lesional drug administration and surgical treatment for oral submucous fibrosis - MEDCT

Government Dental College and Hospital Nagpur0 个研究点目标入组 225 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•Oral submucous fibrosis patients who agrees to participate in the clinical trial and assures to cooperate to undergo the intervention and ready to come for the follow up visits.

•1. Patients with istory of systemic disease with hepatic, respiratory, renal, cardiac or haematological disease.
•2. Patients with presence of any malignancy associated.
•3. Patient with persistent infection or severe
•infection in the last 3 months.
•4. Patient who cannot be relied upon to comply or who are unwilling to sign informed consent.
•5. Patients requiring treatment during the study period with drugs not permitted by the study protocol.

发起方

Government Dental College and Hospital Nagpur