Pain Relief In Irritable Bowel Syndrome
NCT02573844 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2021-08-09
Summary
The purpose of this study is to determine whether Proklama is effective in significative reduction of pain, other symptoms IBS's related, and improves quality of life concerning IBS disease.
Conditions
- Irritable Bowel Syndrome
Interventions
- DRUG
-
Proklama
- DRUG
Sponsors & Collaborators
-
Geophyt S.r.l.s.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-31
- Primary Completion
- 2017-10-31
- Completion
- 2018-06-30
Countries
- Italy
Study Locations
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