Condition 1: Morbid obesity. Condition 2: Bariatric surgery. Morbid (severe) obesity due to excess calories Bariatric surgery status
Conditions
Interventions
Intervention 1: Intervention group: The first group received the probiotic tablets (Familact Co.) daily and started receiving medication one week after surgery until 6 months after surgery.After 4 m
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: BMI = 45 kg/m2 35 =BMI =40 kg/m2 associated with comorbidity
Exclusion criteria
Exclusion criteria: having evidence of chronic gastrointestinal, hepatic or renal disorders having evidence of chronic hepatic disorders having evidence of chronic renal disorders Pregnancy Breastfeeding in women Recieving antibiotics, probiotics or probiotic enriched foods, non-steroid anti-inflammatory drugs (NSAID) or insulin within 4 weeks before the study initiation. History of gastrointestinal surgeries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gastrointestinal Function. Timepoint: start receiving medication 1 week after surgery and start investigation, 5week after surgery, 9weeks after surgery, 12 week after surgery then 6 month after surgery. Method of measurement: Using of Gastrointestinal Quality of Life index questionnaire.;Blood sugar. Timepoint: Before surgery and after surgery for up to 6 months. Method of measurement: Blood test.;Liver enzyme. Timepoint: Before surgery and after surgery for up to 6 months. Method of measurement: Blood test.;Triglyceride. Timepoint: Before surgery and after surgery for up to 6 months. Method of measurement: Blood test.;HbA1C. Timepoint: Before surgery and after surgery for up to 6 months. Method of measurement: Blood test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamid Melali
Esfahan University of Medical Sciences
Outcome results
None listed