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Determination and comparison of urine oxalate after different bariatric surgery

Not Applicable
Recruiting
Conditions
Obesity.
Obesity
Registration Number
IRCT20171118037525N1
Lead Sponsor
Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
105
Inclusion Criteria

Informed consent to participate in research
need to bariatric surgery based on ASMBS(American society for metabolic and bariatric surgery)
age between 18-60 years old

Exclusion Criteria

History of the diseases that may be associated with hyperoxaluria such as Diabetes mellitus, IBD, primary hyperoxaluria, hyperparathyroidism, chronic diarrhea, short bowel syndrome, liver disease, thyroid disease, immunological diseases, cancers, chronic renal failure, urinary tract infections, pregnancy and lactation based on patient history and cases
taking Hydrochlorothiazide medications
taking drugs that affect oxalate or calcium oxalate supersaturation
Lack of cooperation
pregnancy after surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
24 hour urine oxalate. Timepoint: Before the intervention, 1 month after the intervention, 4 months after the intervention and 7 months after the intervention. Method of measurement: Enzymatic method.
Secondary Outcome Measures
NameTimeMethod
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