Obesity Trial, Recruiting NCT07574723 Sponsor: Dasman Diabetes Institute Condition: Obesity
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Obesity Trial, Recruiting

NCT07574723
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 years or older
  • People with a body mass index (BMI) of 27 or above at the time of screening, who have tried dieting to lose weight without success
  • People who have not been diagnosed with diabetes
  • People who are able to read, understand, and sign a consent form
  • People who are able to have a DEXA scan (a type of body composition scan)

Who may not be able to join:

  • People with a history of type 1 or type 2 diabetes
  • People whose body weight has changed by more than 5 kg (11 lbs) in the 90 days before screening, based on their own report
  • People who have taken any medication for weight loss in the 90 days before screening
  • People who have had, or are planning to have, weight-loss surgery or a weight-loss device during the trial period (some past procedures may be allowed if completed more than 1 year before screening — confirm with trial site)
  • People with an uncontrolled thyroid condition, based on a blood test result outside the accepted range at screening
  • People who have had a diagnosis of major depression within the past 2 years
  • People who have been diagnosed with a severe psychiatric condition such as schizophrenia or bipolar disorder
  • People who score 15 or higher on a standard depression questionnaire (called the PHQ-9) at screening
  • People who have ever attempted suicide at any point in their life
  • People who have shown suicidal behaviour in the 30 days before screening
  • People who have used certain non-herbal traditional medicines with unknown ingredients within the past 90 days before screening
  • People who have had acute pancreatitis (sudden inflammation of the pancreas) in the 180 days before screening
  • People with a history of ongoing (chronic) pancreatitis
  • People who, or whose close blood relatives, have a personal history of a condition called multiple endocrine neoplasia type 2 or medullary thyroid cancer
  • People with severely reduced kidney function, based on a blood test at screening
  • People who have been diagnosed with cancer in the past 5 years (certain minor skin cancers may be allowed — confirm with trial site)
  • People who have had a heart attack, stroke, unstable chest pain requiring hospitalisation, or a mini-stroke (transient ischemic attack) in the 60 days before screening
  • People who have been classified as having the most severe level of heart failure (New York Heart Association Class IV)
  • People who have a major surgery planned during the trial period (minor procedures may be acceptable — confirm with trial site)
  • People with known or suspected alcohol or recreational drug misuse
  • People who are known to be allergic or sensitive to the trial treatment or similar products
  • People who have previously signed a consent form for this same trial
  • People who have taken part in another clinical trial within 90 days before screening
  • Women who are pregnant, breastfeeding, planning to become pregnant, or who are able to become pregnant and are not using a highly effective form of contraception
  • People whose circumstances or health conditions, in the opinion of the trial doctor, could put their safety at risk or affect their ability to follow the trial requirements (confirm with trial site)

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 15 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Dasman Diabetes Institute
Registry
ClinicalTrials.gov
Start date
15 May 2026
Est. completion
15 May 2029

Where this trial is recruiting

Kuwait

Primary endpoints

Vomiting episodes per patient assessed using the Modified Index of Nausea, Vomiting, and Retching (M-INVR)

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: 15 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