Obesity Trial, Recruiting NCT07654179 Sponsor: Riphah International University Condition: Obesity
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Obesity Trial, Recruiting

NCT07654179
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older, of any gender
  • People who have been diagnosed with recurring (repeat) depression, classified under the international disease code ICD-11 (6A71)
  • People whose body weight falls into the overweight or obese range using the Asian measurement standard (BMI under 23)
  • People who score at or above a certain level on standard depression questionnaires (BDI score of 13 or higher, or PHQ score of 4 or higher)
  • People who have either never taken antidepressant medication, have been off antidepressants for at least 2 weeks before joining, or did not take antidepressants in the 7 days before joining — note that stopping a medication that is currently working, just to join this trial, is not permitted
  • People taking non-psychiatric medications, provided that medication and dosage have been stable for at least 14 days before joining, with no recent changes in dose or frequency

Who may not be able to join:

  • People under 18 years of age
  • People with dementia or significant cognitive impairment that would prevent them from completing self-reported questionnaires
  • People who have other health conditions such as high blood pressure or chronic kidney disease, if they are currently taking medication for those conditions (confirm with trial site)
  • People who are employees, family members of employees, or otherwise personally connected to the research team or trial site
  • People who have participated in another interventional clinical trial within the 6 months before this trial, or are currently in another trial
  • People who have previously tried antidepressants included in this study without any benefit
  • People who have given birth within the 6 months before joining, or who are currently breastfeeding
  • People who have received ketamine, certain older antidepressants called irreversible MAO inhibitors (such as tranylcypromine), electroconvulsive therapy (ECT), or other stimulation-based treatments during their current episode of depression
  • People diagnosed with dementia or assessed as having moderate to severe general cognitive impairment
  • People who meet clinical criteria for alcohol use disorder or substance use disorder, or whose drug screening test comes back positive (except for benzodiazepines or opiates)
  • People with a known allergy or medical reason to avoid the antidepressants used in the study
  • People with a history of suicidal tendencies
  • People with uncontrolled liver, kidney, or heart disease
  • People with diabetes
  • People with untreated underactive thyroid (hypothyroidism)
  • People with a history of heart attack or stroke
  • People with symptomatic peripheral arterial disease (reduced blood flow to the limbs causing symptoms)
  • People with a hereditary condition causing very high cholesterol levels (monogenic familial hypercholesterolemia)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Afifa,Siddique, PhD Scholar, MBBS, M.Phil, Islamic International Medical College, Riphah International University

Phone: +923175441910

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
17 June 2026
Est. completion
11 June 2027

Where this trial is recruiting

🇵🇰 Pakistan

Primary endpoints

Change in Severity of the depression; Change in BMI

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov