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| ID | Type | Description | Link |
|---|---|---|---|
| 1U19AT003266-01 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| Chinese University of Hong Kong | OTHER |
| National Center for Complementary and Integrative Health (NCCIH) | NIH |
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The purpose of this study is to determine whether a 20- herb formulation, as a well characterised extract, is efficacious in treating irritable bowel syndrome (IBS) and also to identify efficacious and safe dosage of the formulation in treating IBS.
The Specific aims of the project are:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 20-herb formulation | Active Comparator | Active herb |
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| Placebo | Placebo Comparator | Placebo herb formulation |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 20-herb formulation | Drug | Two daily dosages will be investigated. The lowest dosage condition will be 17gm daily, followed by an escalation to 34gm. Participants will be treated for 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Global IBS symptom improvement | The primary endpoint for this study is the efficacy at the 8 week followup visit of the herbal formulations, which is defined by the patient's global assessment of the IBS symptoms. | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| The Bowel Symptom Scale (BSS): | The Bowel Symptom Scale will be used to assess changes in individual IBS and global IBS symptoms during the course of illness. | 8 weeks |
| SF-36 | Quality of Life generic (SF-36), will be used for assessment of quality of life in response to treatment. |
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Inclusion Criteria:
Age 18- 75
All IBS patients attending the Gastroenterology Clinic of the Prince Of Wales Hospital of Hong Kong.
IBS diagnosed by Rome III criteria:
Recurrent abdominal pain or discomfort at least three days per month in the previous three months
Symptoms onset at least six months prior to diagnose
Pain or discomfort associated with two or more of the following:
Normal colonic evaluation (colonoscopy or barium enema) in past 5 years
No "global symptom improvement" as rated by patients (see below) at screening and during the two- week run- in period to baseline
Normal full blood count, liver function test and renal function test.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Brian M Berman, MD | University of Maryland | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Medical Gastroenterelogy Clinic Of the Prince Of Wales, Chinese University of Hong Kong | Shatin | Hong Kong |
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| ID | Term |
|---|---|
| D043183 | Irritable Bowel Syndrome |
| ID | Term |
|---|---|
| D003109 | Colonic Diseases, Functional |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D005767 | Gastrointestinal Diseases |
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| Placebo | Drug | Placebo herb formulation |
|
| 8 weeks |
| IBS-QoL | Disease-specific (IBS-QoL) will be used for assessment of quality of life in response to treatment. | 8 weeks |
| D004066 | Digestive System Diseases |