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Evaluation of efficacy of Dawa e Dhayabitus in Diabetes mellitus type 2

A randomized, parallel group, open label, active controlled clinical study to evaluate safety and efficacy of Dawa-i-Dhayabitus in Dhayabitus Harr Qism Thani (Diabetes Mellitus Type 2) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077509
Enrollment
60
Registered
2024-11-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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: Daw ?’-i-Dhay ?bi?us: Dose & Route of Administration: 2.5g Safuf (Powder) twice daily orally with water Duration of therapy:12 weeks Control Intervention1: Tablet Metformin: Dose: 500mg

Sponsors

National Research Institute Of Unani Medicine for Skin Disorders
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Fasting Blood Glucose (FBG) Levels between 126 and 150 mg/dL   (after 8-12 hours of fasting)  or  Post-Prandial Blood Glucose (PPBG) Level between 200 and 250 mg/dL  (after 2 hours of ingestion of meal)  Glycated Haemoglobin (HbA1c) between 6.5% and 8%   Patients willing to sign the written informed consent    with / without  Presence of any of the following symptoms of Dhay ?bi?us ? ?rr Qism Th ?ni (Type 2 Diabetes Mellitus):    U?ash Mufri? (Polydipsia)   Kathrat-i-Bawl (Polyuria)   Kathrat-i-Ishtiha (Polyphagia)   Bawl Layli (Nocturia)  Burning sensation in palms and soles  Naqs al-Wazn (Weight Loss)   I’ya (Fatigue)   D?u‘f-i-‘Am (General Weakness)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Change in Fasting Blood Glucose (FBG), Post Prandial Blood Glucose (PPBG), HbA1c from baseline to post treatment at 12 weeksTimepoint: At baseline, 2, 4, 6, 8, 10 and 12 weeks

Secondary

MeasureTime frame
Improvement in symptoms on VAS from baseline to post treatment at 12 weeksTimepoint: At baseline, 2, 4, 6, 8, 10 and 12 weeks

Countries

India

Contacts

Public ContactDr Saiyed Fatema Anjum

National Research Institute of Unani Medicine for Skin Disorders Hyderabad

drnasar.nriumsd@gmail.com8328446962

Outcome results

None listed

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