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Comparative study for the effect of Unani formulation and allopathic drug in the treatment of Type 2 Diabetes Mellitus

Effect of Satt-i Gilo in management of DhayÄ?bīṭus Sukkari Qism ThÄ?ni(T2DM) A Randomised Standard Control Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/030141
Enrollment
40
Registered
2020-12-30
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: Satt-i Gilo capsule: 2 capsules of 500mg twice a day orally for a period of 90 days Control Intervention1: Metformin: 1 Tablet of Metformin 500mg twice a day orally for a period of 90 d

Sponsors

Luqman Unani Medical College Hospital and Research Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-Diagnosed cases of type 2 Diabetes mellitus with blood sugar level: -Fasting blood sugar equal to or more than 126mg/dl to more than 200mg/dl, -Random or post-prandial blood sugar level equal to or more than 200mg/dl to more than 300mg/dl, and -HbA1c equal to or more than 6.5% to 8% 2-Patient ready to participate in the study and ready to follow instructions

Exclusion criteria

Exclusion criteria: -Diagnosed cases of type 2 DM with Fasting blood sugar more than 200mg/dl, Random OR Postprandial blood sugar more than 300mg/dl, and HbA1c more than 8 percent -Patient of type 1 Diabetes mellitus on insulin. -Cases of gestational diabetes mellitus. -Pregnant and lactating women. -Patient with complications like nephropathy, neuropathy, retinopathy, ketoacidosis, lactic acidosis. -Known cases of CAD, PVD, Stroke, liver diseases, hemoglobinopathy, and accelerated hypertension.

Design outcomes

Primary

MeasureTime frame
-HbA1c (Glycosylated hemoglobin) -eAG (Estimated average glucose)Timepoint: At baseline and after 3 months

Secondary

MeasureTime frame
-Fasting blood sugar -Postprandial blood sugar -Diabetes quality of life(DQoL)Timepoint: At baseline, 30 days, 60 days and after completion of study

Countries

India

Contacts

Public ContactMohd Khalid

Luqman Unani Medical College Hospital and Research Center

drdafedar1@gmail.com9032786832

Outcome results

None listed

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