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Comparison of two methods with and without creasing of part of the stomach in patients with morbid obesity

Phase 2
Recruiting
Conditions
Morbid obesity.
Body mass index (BMI) 40.0-44.9, adult.
Z68. 41
Registration Number
IRCT20201201049551N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Age 18-65 years
Obesity with a BMI of more than 35 with comorbidity disease or more than 40 kg / m2
Obesity with comorbidity diseases
Patients with consent to participate in the study

Exclusion Criteria

Debilitating diseases, including cancer, tuberculosis, AIDS
Having diseases that limit patient-physician communication, such as Alzheimer's
Recorded history of mental illness (major depression or uncontrolled psychosis)
Drug and alcohol abuse
Severe heart disease with risk of anesthesia
Severe coagulopathy
Not accepting nutritional orders
History of gastric surgery or antireflux surgery
High-grade dysplasia in Barrett's esophagus
Severe iron deficiency anemia
Distal lesions of the stomach or duodenum require follow-up
Patients with no consent to participate in the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Weight Loss. Timepoint: Two weeks, 1,2,6, 12 months after surgery. Method of measurement: The rate of weight loss two weeks after surgery is 4%, 1 month after 8%, 3 months after 18%, 6 months after 30%, 12 months after 40% relative to baseline weight.
Secondary Outcome Measures
NameTimeMethod
The amount of ghrelin hormone. Timepoint: Six, 12 months after surgery. Method of measurement: Pg/mL.
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