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probiotics and postoperative weight loss of sleeve surgeries

Effect of probiotics on postoperative weight loss of sleeve surgeries: a randomized trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210817052218N2
Enrollment
60
Registered
2022-08-08
Start date
2022-09-06
Completion date
Unknown
Last updated
2022-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Morbid Obesity. Overweight and obesity

Interventions

Intervention 1: Intervention group: Patients in the intervention group will take one probiotic supplement capsule every day for 12 weeks, and unused capsules should be kept in the refrigerator. Patien

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: patients aged between 18 and 65 years morbidly-obese patients candidates for bariatric surgery , BMI above 40 kg/m2

Exclusion criteria

Exclusion criteria: Chronic damage to the digestive system, liver and kidney Insulin use within 4 weeks before the start of the study and during the study Patients with micronutrient deficiency of vitamin D, folic acid and iron storage Pregnant patients Consuming foods enriched with probiotics within 4 weeks before the start of the study and during the study Corticistreoid consumption within 4 weeks before the start of the study and during the study Taking immunosuppressive drugs within 4 weeks before the start of the study and during the study

Design outcomes

Primary

MeasureTime frame
BMI (body mass index). Timepoint: Before, three and six months after the intervention. Method of measurement: scale.;Fat mass. Timepoint: Before, three and six months after the intervention. Method of measurement: According to the measurement of anthropometric index with the inbody 370 bioimpedance analyzer (Biospace America, Inc.).;Muscle mass. Timepoint: Before, three and six months after the intervention. Method of measurement: According to the measurement of anthropometric index with the inbody 370 bioimpedance analyzer (Biospace America, Inc.).;Excess body weight loss. Timepoint: Before, three and six months after the intervention. Method of measurement: Calculation based on the difference between the patient's weight and the difference between the preoperative weight and the ideal weight.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Hakakzadeh

Shahid Beheshti University of Medical Sciences

ahakakzade@yahoo.com+98 21 23871

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026