Clinical TrialID 931

Effect of Flixweed and Fig on Irritable Bowel Syndrome With Predominant Constipation: a Single Blind Randomized Clinical Trial.

NCT02559245

Irritable Bowel Syndrome Predominant Constipation

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Record Fields

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Clinical Trial Id
931
Evidence Id
931
Core Evidence Id
931
Source Clinical Trial Id
913
Herb2 Clinical Trial Id
HBCT000913
Nct Id
NCT02559245
Title
Effect of Flixweed and Fig on Irritable Bowel Syndrome With Predominant Constipation: a Single Blind Randomized Clinical Trial.
Status
Completed
Phase
Study Result
No
Study Condition
Irritable Bowel Syndrome Predominant Constipation
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
OTHER: Descurainia Sophia|OTHER: Ficus carica
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Single
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
150
Outcome Measure
irritable bowel syndrome constipation predominant symptom, IBS severity score system questionnaires will use for evaluation of IBS-C symptoms at the pre and post-intervention. This tool is validated for use in IBS patients that assess 5 clinically relevant items during past 10-days and including severity of abdominal pain, frequency of abdominal pain, severity of abdominal distention, dissatisfaction with bowel movement and interference of IBS with life in general. Each items was scored with a 100 mm visual analogue scale (VAS)., 4 months
Sponsor Collaborator
Isfahan University of Medical Sciences
Funded By
OTHER
Location
Gastrointestinal Research Center, Isfahan, Iran, Islamic Republic of
Start Date
2015-09
Primary Completion Date
2016-01
Completion Date
2016-01
First Posted
2015-09-24
Results First Posted
Last Update Posted
2018-05-22
Study Document
Study Url
https://clinicaltrials.gov/study/NCT02559245
Title Cn
Title En
Effect of Flixweed and Fig on Irritable Bowel Syndrome With Predominant Constipation: a Single Blind Randomized Clinical Trial.
Bilingual Status
semi_complete