Effect of Metamucil on Bowel Preparation for Colonoscopy
| ISRCTN | ISRCTN76623768 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN76623768 |
| Protocol serial number | N/A |
| Sponsor | Procter and Gamble Company (USA) |
| Funders | Procter and Gamble Company (USA), Wayne State University (USA) |
- Submission date
- 09/12/2003
- Registration date
- 10/12/2003
- Last edited
- 29/08/2007
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Marc Basson
Scientific
Scientific
4646 John R
Detroit
48201
United States of America
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Bowel Preparation for Colonoscopy |
| Intervention | Patients randomised to 4 days of Metamucil versus Placebo prior to consuming a standard lavage, followed by colonoscopy |
| Intervention type | Drug |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Metamucil |
| Primary outcome measure(s) |
Not provided at time of registration |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/01/2003 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 64 |
| Key inclusion criteria | Patients scheduled for colonoscopy using a standard lavage preparation |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/2002 |
| Date of final enrolment | 01/01/2003 |
Locations
Countries of recruitment
- United States of America
Study participating centre
4646 John R
Detroit
48201
United States of America
48201
United States of America
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | Results | 02/02/2004 | Yes | No |