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Treatment of abdominal symptoms in non-complicated

The effect of mesalazine in comparison with placebo in uncomplicated diverticulosis with abdominal symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201606237080N4
Enrollment
120
Registered
2016-07-04
Start date
2016-06-30
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

diverticulosis. Diverticular disease of intestine, Diverticular disease of large intestine without perforation or abscess, Diverticular disease of both small and large intestine without perforation or abscess, Diverticular disease of intestine, part unspecified, without

Interventions

Intervention 1: 3 Pills of mesalazine 500 mg in a day (1.5 gr daily) for 1 week in each month, for 3 months. Intervention 2: 3 pills of placebo, daily, for 1 week in each month, for 3 months.
Treatment - Drugs
3 Pills of mesalazine 500 mg in a day (1.5 gr daily) for 1 week in each month, for 3 months.
3 pills of placebo, daily, for 1 week in each month, for 3 months.

Sponsors

Vice Chancellor for research of Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the patients between 40 to 70 years old that have chronic abdominal pain and colonoscopy or barium enema are done for them and based on clinical symptoms and colonoscopy and radiology; the diagnosis of diverticulosis is arisen for them. Exclusion criteria: age below 40 and above 70; patients with history of abdominal surgery; musculoskeletal disease; spinal disorders; gallbladder stone; renal stone; bowel motility disease and inflammatory bowel disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bloat. Timepoint: At the start of intervention, 1 month later, 2 months later, 3 months later. Method of measurement: questionnaire.;Mucus discharge. Timepoint: At the start of intervention, 1 month later, 2 months later, 3 months later. Method of measurement: Number of defecation in a week.;Constipation. Timepoint: At the start of intervention, 1 month later, 2 months later, 3 months later. Method of measurement: Number of defecation in a week.;Abdominal pain. Timepoint: At the start of intervention, 1 month later, 2 months later, 3 months later. Method of measurement: VAS( score 0 to 10).

Secondary

MeasureTime frame
Diverticulitis. Timepoint: At the start of the intervention, after 2 month of treatment. Method of measurement: Clinical symptoms and signs and CT scan.;Bleeding. Timepoint: At the start of the intervention, after 2 month of treatment. Method of measurement: See bleeding.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaede Abdinzade

Babol University of Medical Sciences

abedinzadeh.ma@yahoo.com+98 11 3219 7667

Outcome results

None listed

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