THE EFFECT OF FAST WEIGHT EFFICIENCY AFTER LAPAROSCOPIC SLEEVE GASTRECTOMY ON THE COBB ANGLE IN MORBID OBESE PATIENTS
NCT ID: NCT04844320
Last Updated: 2021-04-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
90 participants
INTERVENTIONAL
2021-04-01
2021-12-01
Brief Summary
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The aim of this study is to reveal the Cobb angle change in morbidly obese patients who achieved rapid weight loss after obesity surgery; To investigate the effect of weight loss on vertebral anatomy.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
Patients in these 3 groups will be randomized on www.randomisor.org. In these 3 groups, cobb angle measurements will be made on the PA chest radiographs taken at the preoperative, postoperative 1st year and postoperative 2nd year controls. Patient satisfaction questionnaires will be conducted to compare pre- and postoperative complaints such as low back pain, back pain, and neck pain in all patients. The change in cobb angles will be determined according to the weight loss ratio (% EWL) of the patients.
TREATMENT
NONE
Study Groups
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> 50 %EWL
Postoperative weight loss in first year \> 50 % EWL
Cobb angle measurements
PA Chest x-rays will be taken in all patients in the preoperative, postoperative 1st year and 2nd year
50 - 25 % EWL
Postoperative weight loss in first year 25 - 50 % EWL
Cobb angle measurements
PA Chest x-rays will be taken in all patients in the preoperative, postoperative 1st year and 2nd year
< 25 % EWL
Postoperative weight loss in first year \< 25 % EWL
Cobb angle measurements
PA Chest x-rays will be taken in all patients in the preoperative, postoperative 1st year and 2nd year
Interventions
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Cobb angle measurements
PA Chest x-rays will be taken in all patients in the preoperative, postoperative 1st year and 2nd year
Eligibility Criteria
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Inclusion Criteria
* Patients with a diagnosis of morbid obesity, body mass index\> 40
Exclusion Criteria
* Patients hospitalized for more than 10 days due to postoperative complications
16 Years
90 Years
ALL
No
Sponsors
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Fatih Sultan Mehmet Training and Research Hospital
OTHER
Responsible Party
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ANIL ERGIN
MD. Anil Ergin
Locations
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Anıl Ergin
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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DR. ANIL ERGIN
Identifier Type: -
Identifier Source: org_study_id
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