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Clinical Trials/NCT05759442
NCT05759442CompletedNot Applicable

Clinical Efficacy and Safety of Metformin Versus Apple Cider Vinegar (ACV) in Prediabetics

Bahria University1 site in 1 country46 target enrollmentStarted: January 1, 2023Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
46
Locations
1
Primary Endpoint
Glycated Hemoglobin

Study Overview

Brief Summary

The goal of this clinical trial is to compare efficacy and safety of metformin versus apple cider vinegar in prediabetics . The main question[s] it aims to answer are:

  • Efficacy of metformin versus apple cider vinegar in prediabetics
  • Safety of metformin versus apple cider vinegar in prediabetics

Researchers will compare group of prediabetics taking metformin with group of prediabetics taking apple cider vinegar to see if there is difference in safety and efficacy..

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
17 Years to 40 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Males and Female
  • •17-40 years age
  • •Body Mass index (BMI) overweight and obese
  • •FBS (100-125 mg/dl)
  • •HBA1c 5.7% to 6.4%

Exclusion Criteria

  • •Concomitant medical problems as established diabetes, hepatic or renal insufficiencies etc.
  • •Known allergy or intolerance to metformin or apple cider vinegar

Arms & Interventions

Apple cider vinegar

Active Comparator

Apple Cider Vinegar 15ml per day diluted in 200 ml of water for 12 weeks

Intervention: Apple cider vinegar (Dietary Supplement)

Metformin

Active Comparator

Tablet Metformin HCl 500 mg per oral twice daily for 12 weeks

Intervention: Metformin Hydrochloride (HCL) (Drug)

Outcomes

Primary Outcomes

Glycated Hemoglobin

Time Frame: 12 weeks

Change in glycosylated hemoglobin (HbA1c ) in percent

Fasting Blood Sugar

Time Frame: 12 weeks

Change in fasting blood sugar (FBS) in mg/dL

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Shizma Junejo

Senior Lecturer Pharmacology Department

Bahria University

Study Sites (1)

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