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NCT Number: NCT06841497

Safety and Efficacy Assessment of Unani Formulation 'Dolabi' in Management of Diabetes Mellitus Type II

Diabetes is a chronic health condition that affects millions of people worldwide. In recent years, Pakistan has witnessed a significant increase in the prevalence of diabetes, making it a major public health concern. To address this growing problem, conducting clinical trials on diabetes in Pakistan is of utmost importance. Clinical trials play a crucial role in advancing medical knowledge, improving patient care, and finding effective treatments for diabetes.

This research aims to assess the safety and effectiveness of the Unani formulation Dolabi in treating type II diabetes mellitus. The study consists of two phases: a pre-clinical phase, which involves acute and subacute oral toxicity testing on animal models, and a clinical phase, which includes a single-blind, single-arm, multicenter, phase II clinical trial conducted at Shifa ul Mulk Memorial Hospital-Hamdard University and Haidery Herbal Care-North Nazimabad to evaluate its clinical efficacy.

Diabetes management plays a vital role in effectively controlling the disease and minimizing its complications. Lifestyle management plays significant role in managing blood glucose levels in all age and gender segments. Medications are prescribed to regulate blood glucose levels when lifestyle changes alone are insufficient. Regular monitoring of blood sugar levels, along with other important parameters like blood pressure and cholesterol, helps individuals with diabetes to track their progress and make necessary adjustments to their treatment plans.

Dolabi is a time tested formulation of HLWP and it is being used clinically for more than 05 years at Hamdard Matabs all around Pakistan and clinically found satisfactory. The current study is designed in accordance with ICH GCP E6 protocols as approved by WHO and DRAP. It will enable us to present this safer and locally produced combination for the large community suffering with this condition in improving their lives.

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This study is active but is not currently recruiting participants.

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Key information

Age range

30 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Shifa Ul Mulk Memorial Hospital-Hamdard University

Karachi, Sindh, 74600, Pakistan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects having Type II Diabetes Mellitus.
  • Subjects having raised FBS above 120 mg/dl and HbA1C level 6.7 or above.
  • Subjects over 30 years of age.
  • Subjects agree to use study medicine throughout the study.

Exclusion criteria

  • Subjects suffering from chronic liver diseases and kidney failure.
  • Subjects currently taking any hypoglycemic agent(s).
  • Subjects suffering from any type of cancer and any other comorbid condition.
  • Subjects having history of adverse drug reaction.
  • Pregnant and Lactating mother.

Treatment and study plan

Dolabi

Other

herbal remedy for DM II

Primary outcomes

  1. Blood Sugars

    Time frame: 12 weeks

    Fasting Blood sugars at baseline and the end of treatment will be assess in (mg/dl).

  2. HbA1C (Glycosylated Hemoglobin)

    Time frame: 12 weeks

    Monitoring of HbA1C at baseline and at the end of treatment. the values of HbA1C will be assess in percentage (%).

Sponsors and collaborators

Lead sponsor

Hamdard University

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 24, 2025
Registry last updated
Feb 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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