Actively Recruiting

Phase 4
Age: 18Years - 45Years
All Genders
NCT06707012

Efficacy of Metformin as an Adjunct to Standard Antidepressant Therapy in Treating Depression Among Obese Patients

Led by Fazaia Ruth Pfau Medical College · Updated on 2025-09-19

140

Participants Needed

2

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To evaluate the efficacy of metformin as an adjunct therapy in improving depressive symptoms and metabolic markers in newly diagnosed obese depressed patients on standard antidepressant therapy. investigator will compare between Two groups 1\. metformin group 2 placebo group Primary outcome measure will be the improvement in depressive symptoms, indicating by a reduction in Hamilton Depression Rating Scale (HAM-D) scores. Secondary outcome measures will include the assessment of oxidative stress markers, specifically by measuring the increase in enzymatic activity of superoxide dismutase, catalase, and glutathione peroxidase Investigators hypothesize that the addition of metformin to standard antidepressant treatment will result in a significant reduction in symptoms of depression among newly diagnosed obese individuals.

CONDITIONS

Official Title

Efficacy of Metformin as an Adjunct to Standard Antidepressant Therapy in Treating Depression Among Obese Patients

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 and under 45 years
  • Both male and female genders
  • Body mass index (BMI) greater than 25
  • Newly diagnosed cases of mild to severe depression
  • HbA1c less than 5.7% (non-diabetic range)
Not Eligible

You will not qualify if you...

  • Existing diabetes
  • Acute illnesses such as acute kidney injury, recent heart attack, or acute liver injury
  • Intellectual disabilities or inability to understand the study
  • Psychiatric disorders other than depression
  • Chronic kidney disease with eGFR below 45 mL/min/1.73 m²
  • Use of any psychotropic medication within the past 6 months

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Fazaia Rurh Pfau Medical College

Karachi, Sindh, Pakistan, 75120

Actively Recruiting

2

Fazaia Ruth Pfau Medical College

Karachi, Sindh, Pakistan, 75120

Actively Recruiting

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Research Team

S

Sadia khan, MBBS

CONTACT

A

Asghar Mehdi, MBBS,PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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