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Compares treatment options for Obesity
Official title Binge Eating, Depression and Anxiety Outcomes After Sleeve Gastrectomy Versus Gastric Bypass: A Cohort Study
ClinicalTrials.gov ID: NCT07600411
What this study is testing
- What it's testing
- The goal of this clinical trial is to learn if the type of weight-loss surgery (sleeve gastrectomy or gastric bypass) affects binge eating, depression, and anxiety in adults with severe obesity. The main questions it aims to answer are: Does sleeve gastrectomy lead to different changes in binge eating compared with gastric bypass?
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 60
You may be able to join if
- Age between 18 and 60 years
- Body Mass Index (BMI) ≥ 35 kg/m² without comorbidities, OR BMI ≥ 30 kg/m² with at least one obesity-related medical comorbidity (e.g., type 2...
- Patient is generally fit for laparoscopic surgery and general anesthesia as determined by preoperative evaluation
- Patient agrees to comply with postoperative lifestyle changes (dietary modifications and follow-up schedule)
- Willing and able to provide written informed consent
You likely can't join if
- Age \ 60 years
- Inability or unwillingness to adhere to postoperative lifestyle changes
- Contraindication to surgery: American Society of Anesthesiologists (ASA) class IV or higher
- History of receiving radiotherapy or chemotherapy for cancer treatment
- Active substance use disorder or uncontrolled severe psychiatric illness that would impair ability to comply with study procedures (e.g., active...
- Pregnant or breastfeeding women (pregnancy test performed preoperatively per institutional protocol)
See the full eligibility criteria
- Age between 18 and 60 years
- Body Mass Index (BMI) ≥ 35 kg/m² without comorbidities, OR BMI ≥ 30 kg/m² with at least one obesity-related medical comorbidity (e.g., type 2 diabetes, hypertension, obstructive sleep apnea, dyslipidemia)
- Patient is generally fit for laparoscopic surgery and general anesthesia as determined by preoperative evaluation
- Patient agrees to comply with postoperative lifestyle changes (dietary modifications and follow-up schedule)
- Willing and able to provide written informed consent
- Age \ 60 years
- Inability or unwillingness to adhere to postoperative lifestyle changes
- Contraindication to surgery: American Society of Anesthesiologists (ASA) class IV or higher
- History of receiving radiotherapy or chemotherapy for cancer treatment
- Active substance use disorder or uncontrolled severe psychiatric illness that would impair ability to comply with study procedures (e.g., active psychosis, severe suicidal ideation)
- Pregnant or breastfeeding women (pregnancy test performed preoperatively per institutional protocol)
- Previous bariatric surgery (revisional surgery excluded)
- Untreated thyroid disorder (e.g., hypothyroidism or hyperthyroidism)
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Al-Manial Cairo, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 60 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Al-Manial Cairo, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.