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临床试验/CTRI/2025/11/097024
CTRI/2025/11/097024尚未招募2 期

A Randomized, open-label, parallel-group, active controlled clinical study to evaluate the safety and efficacy of a Unani formulation compared with Metformin in patients with Dhayabitus Harr [Type 2 Diabetes Mellitus (G-2)]

Central Council for Research in Unani Medicine1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年11月20日最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
100
试验地点
1
主要终点
Changes in the fasting and postprandial blood glucose

研究概览

简要总结

Study RationaleThe Unani System of Medicine focuses on prevention through lifestyle modification dietary management and prophylactic interventions and enhances the immune system to fight against any disease. No specific drug is available for diabetes mellitus instead the drug is used to control the glucose level in the body and manage signs and symptoms of diabetes mellitus. The most commonly used drugs are Oral Hypoglycaemic Drugs (OHD) such as Sulphonylureas (SUs) and Biguanides (BGs). However these drugs have several adverse effects, and long term use of these drugs accumulate adverse effects that may be life threatening and in most cases affect the patient’s quality of life. The Unani drugs are natural and well tolerated by the body and produce fewer side effects than synthetic drugs. Several single and compound formulations are mentioned in the Unani literature which may maintain the body’s blood glucose level and vis-a-vis improve life quality. Therefore Unani formulations with ingredients having hypoglycemic activity may prove beneficial in the effective management of Diabetes mellitus, type 2.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
25.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Clinically diagnosed cases of Type 2 diabetes for at least 6 months prior to screening.
  • HbA1c level equal to or more than 6.5 % at screening.
  • Willing and able to provide written informed consent.
  • Willing to comply with the protocol requirements.

排除标准

  • 未提供

结局指标

主要结局

Changes in the fasting and postprandial blood glucose

时间窗: Changes in the fasting and postprandial blood glucose | Changes in the HbA1C | from baseline to post-treatment at 90 days.

Changes in the HbA1C

时间窗: Changes in the fasting and postprandial blood glucose | Changes in the HbA1C | from baseline to post-treatment at 90 days.

from baseline to post-treatment at 90 days.

时间窗: Changes in the fasting and postprandial blood glucose | Changes in the HbA1C | from baseline to post-treatment at 90 days.

次要结局

  • changes in the VAS score for clinical findings.(Changes in the biomarkers.)

研究者

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

Dr Mohammad Zakir

National Research Institute of Unani Medicine for Skin Disorders

研究点 (1)

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