Trial Details
RECRUITINGBasic Information
| Clinical ID | c650 |
|---|---|
| Identifier | NCT06271538 |
| Trial Title | Evaluation of Efficacy of Skål Pro Powder on Symptoms of Irritable Bowel Syndrome |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| Conditions | Irritable Bowel Syndrome|Gastrointestinal Diseases|Colonic Diseases, Functional|Intestinal Disease|Digestive System Disease|Pathologic Processes|Colonic Disease|Disease |
| Interventions | COMBINATION_PRODUCT: Skal Pro|OTHER: Placebo |
Participant Information
| Sponsor | EP Plus Group Sdn Bhd |
|---|---|
| City | Kelantan |
| Country/Region | Malaysia |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE4 |
Time Information
| Start Date | 2024-10-17 |
|---|---|
| Primary Completion Date | 2025-07-31 |
| Completion Date | 2025-11-30 |