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Probiotics Bismuth Subsalicylate and Abdominal Bloating

Evaluation and comparison of the therapeutic effects of probiotics, Bismuth subsalicylate and placebo in patients with abdominal bloating in patients referring to gastrointestinal clinic in Khorshid hospital.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200601047621N1
Enrollment
100
Registered
2020-06-18
Start date
2020-07-29
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

Abdominal Bloating. Flatulence

Interventions

Intervention 1: Intervention group1: Probiotic recipient. Patients on this group receive Familact probiotic tablets from the Zist-takhmir company, containing 7 strains of bacteria (lactobacilli, bifid

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: All of the Patients with Abdominal Bloating Age between 20 and 50 years Feeling bloated for at least 3 days a month for the last 3 months The first experience of bloating more than 6 months ago

Exclusion criteria

Exclusion criteria: Any history of chronic inflammatory disease or structural disease of the gastrointestinal tract Any serious physical problems or illness, such as inflammation or malignancy Use of calcium channel blockers in the last 3 months Severe stress in the last 6 months Positive family history for Colon Concert History of inflammatory diseases Lactase deficiency disease Celiac disease

Design outcomes

Primary

MeasureTime frame
Abdominal Bloadting. Timepoint: Before the start of the study, 2 weeks after the start of the study, 4 weeks after the start of the study, 6 weeks after the start of the study and 8 weeks after the start of the study. Method of measurement: Questionnaire for bloating and IBS-QOL questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Soheilipour

Esfahan University of Medical Sciences

maryamsoheilip@med.mui.ac.ir+98 31 3729 4225

Outcome results

None listed

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