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Clinical Study to Evaluate Qurs-e-Zayabitus Khas and Qurs-e-Tabasheer Over Metformin in Type-2 Diabetes Mellitus

A Single Blind, Randomised, Active Controlled Clinical Study to Evaluate the Efficacy and Safety of a Combination of Unani Drugs â?? Qurs-e-Zayabitus Khas and Qurs-e-Tabasheer in DhayÄ?bīṭus HÌ£Ä?rr Qism ThÄ?nÄ« (Type 2 Diabetes Mellitus) - PGAN

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/04/018670
Enrollment
60
Registered
2019-04-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E119- Type 2 diabetes mellitus without complications

Interventions

Intervention1: Group A (Qurs-e-Zayabitus Khas and Qurs-e-Tabasheer): Qurs-e-Zayabitus Khas and Qurs-e-Tabasheer will be prepared in a single batch, according to the standard method described in Nation

Sponsors

Central Research Institute of Unani Medicine Hyderabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of any sex aged 30-65 years Fasting plasma glucose levels between 126 and 175 mg/dL or Post Prandial plasma glucose levels between 200 and 250 mg/dL (2 hours after ingestion of 75 gm of glucose in 300 ml of water) or HbA1c level between 6.5 and 8% and Presence of any of the following symptoms and signs of diabetes mellitus (2 hours after ingestion of 75 gm of glucose in 300 ml of water) or HbA1c level between 6.5 and 8% and Presence of any symptoms and signs of diabetes mellitus

Exclusion criteria

Exclusion criteria: Subjects with FPG level >175 mg/dL and/ or PP plasma glucose level >250 mg/dL and/ or HbA1c >8% Subjects on Insulin therapy Type 2 DM with complications/ Secondary DM/Type 1 DM Significant pulmonary/ cardiovascular/ hepato-renal dysfunction Known cases of immunocompromised states (HIV/ AIDS, etc.)/ Malignancies Obese subjects (BMI >30) Pregnant and lactating women Drug addicts/Alcoholics Patient not willing to attend treatment schedule regularly

Design outcomes

Primary

MeasureTime frame
1.Reduction in Fasting and PP plasma glucose (2-hPG) level 2.Decrease in HbA1c level by more than equal to 1 percent as compared to baseline 3.Improvement in the following symptoms of DhayÄ?bīṭus HÌ£Ä?rr Qism ThÄ?nÄ« (Type 2 Diabetes Mellitus) on 0-100mm Timepoint: At baseline, 2wk, 4wk, 6wk, 8wk, 10wk, and 12wk

Secondary

MeasureTime frame
Hemogram, LFT, RFT, FPG, Urine R/M examinationTimepoint: At baseline and 8th followup

Countries

India

Contacts

Public ContactTasleem Ahmed

Central Research Institute Of Unani Medicine,

ccrumhqrsnd58@gmail.com8700027178

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026