effect of almond fruit in IBS patients

Not Applicable

• Conditions: irritable bowel syndrome.; Irritable bowel syndrome with diarrhoea

• Registration Number: IRCT2017070234861N1
• Lead Sponsor: Kerman University of Medical Sciences, Vice Chanellor of Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Criteria for entering the study are the presence of Rome III cirrhosis, which include: pain; recurrent abdominal discomfort for at least three days a month in the last three months, with the elimination of two of the following: defecation with bowel movements; The onset of symptoms with a change in the frequency of bowel movements; the onset of symptoms along with a change in the stool shape;
Exclusion criteria
withdrawal criteria for patients who did not take the medicine on a regular basis; patients who did not complete the assessment form completely

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain location. Timepoint: 20 day. Method of measurement: Data validation form.;Pain consequency. Timepoint: days 0 and 20. Method of measurement: data evaluation form.;Pain consequency. Timepoint: days 0 and 20. Method of measurement: data evaluation form.;Pain intensity. Timepoint: days 0 and 20. Method of measurement: data evaluation form.

Secondary Outcome Measures

Name	Time	Method
Buttal in daily functio. Timepoint: 20 day. Method of measurement: Data validation form.;.pain intensity. Timepoint: days 0 and 20. Method of measurement: data evaluation form.;Analgesic drug taking. Timepoint: days 0 and 20. Method of measurement: data evaluation form.