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Effect of treatment with mesalamine and bismuth on the symptoms of irritable bowel syndrome.

Efficacy of treatment of bloating dominant irritable bowel syndrome patients by mesalazine and bismuth

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014080814190N4
Enrollment
40
Registered
2014-10-08
Start date
2013-11-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Irritable Bowel Syndrome. Irritable Bowel Syndrome

Interventions

Intervention group: Mesalamine 2 gram daily + bismuth 120 mg daily.
Treatment - Drugs
Intervention group: Mesalamine 2 gram daily + bismuth 120 mg daily

Sponsors

Vice Chancellor for Research and Technology Development, Ahvaz Jondishapur University of Medical Sci
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: symptomatic patients more than 3 months; a normal colonoscopy; rule out celiac in patients; the patient's symptoms did not improve despite the use of conventional regimens for a year. Exclusion criteria: pregnancy or lactation; history of abdominal surgery; opioid analgesics; nonsteroidal anti inflammatory drugs; long term use of antibiotics; history of renal failure; severe liver disease; a history of hypersensitivity to salicylates; being diagnosed with a serious illness.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bloating. Timepoint: At first, second and fourth month of the study. Method of measurement: Patient assessment conducted by questionnaire.;Frequency of daily defecation. Timepoint: At first, second and fourth month of the study. Method of measurement: Patient assessment conducted by questionnaire.;Severity of abdominal pain. Timepoint: At first, second and fourth month of the study. Method of measurement: Patient assessment conducted by questionnaire.

Secondary

MeasureTime frame
Vomiting. Timepoint: At first, second and fourth month of the study. Method of measurement: Patient assessment conducted by questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Atefeh Roumi

Ahvaz Jundishapur University of Medical Sciences

Atefeh.Roumi@gmail.com+98 61 1336 7543

Outcome results

None listed

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