NCT06841497

Brief Summary

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable diabetes-mellitus

Timeline
Completed

Started Jul 2024

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 4, 2024

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

February 17, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 4, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 3, 2025

Completed
Last Updated

February 24, 2025

Status Verified

February 1, 2025

Enrollment Period

1 year

First QC Date

February 17, 2025

Last Update Submit

February 21, 2025

Conditions

Keywords

Diabetes MellitusT2DMMetabolic diseaseInsulin Resistance

Outcome Measures

Primary Outcomes (2)

  • Blood Sugars

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

    12 weeks

  • HbA1C (Glycosylated Hemoglobin)

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

    12 weeks

Study Arms (1)

Effect of Dolabi on DM II

EXPERIMENTAL
Other: Dolabi

Interventions

DolabiOTHER

herbal remedy for DM II

Effect of Dolabi on DM II

Eligibility Criteria

Age30 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shifa Ul Mulk Memorial Hospital-Hamdard University

Karachi, Sindh, 74600, Pakistan

Location

MeSH Terms

Conditions

Diabetes MellitusMetabolic DiseasesInsulin Resistance

Condition Hierarchy (Ancestors)

Glucose Metabolism DisordersNutritional and Metabolic DiseasesEndocrine System DiseasesHyperinsulinism

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 17, 2025

First Posted

February 24, 2025

Study Start

July 4, 2024

Primary Completion

July 4, 2025

Study Completion

October 3, 2025

Last Updated

February 24, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share

Locations