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| Tracking Information | |||||
|---|---|---|---|---|---|
| First Received Date ICMJE | January 9, 2007 | ||||
| Last Updated Date | November 28, 2007 | ||||
| Start Date ICMJE | February 2007 | ||||
| Primary Completion Date | |||||
| Current Primary Outcome Measures ICMJE |
The primary efficacy variable will be the change from baseline to the end of study in the faecal incontinence score (St Mark's) | ||||
| Original Primary Outcome Measures ICMJE |
The primary efficacy variable will be the change from baseline to the end of study in the faecal incontinence score (St Mark’s) | ||||
| Change History | Complete list of historical versions of study NCT00420797 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE | Same as current | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | A Study to Evaluate Topical Phenylephrine Gel in the Management of Faecal Incontinence | ||||
| Official Title ICMJE | A Double-Blind, Randomised, Placebo-Controlled Study to Evaluate Topical 10% Phenylephrine Gel in the Management of Ileal Pouch Anal Anastomosis (IPAA)-Related Faecal Incontinence | ||||
| Brief Summary | The aim of the study is to test the hypothesis that topical application of phenylephrine improves faecal continence and quality of life in subjects with passive faecal incontinence after ileo-anal pouch construction. |
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| Detailed Description | Faecal seepage and even frank incontinence at night can be a problem for approximately 30% of patients who have undergone ileal pouch anal anastomosis (IPAA). Nocturnal seepage may be a problem in patients who do not have gross incontinence, or who may even have no incontinence during the day. Although baseline continence during the day is maintained by involuntary control of the internal anal sphincter, this can be supplemented by voluntary contraction of the external sphincter. While sleeping, this supplementary external sphincter effect is lost and internal anal sphincter tone is reduced, leading to seepage. This is obviously distressing and leads some patients to wear a pad to reduce the soiling that may occur. The primary objective is to determine the effect of 10% phenylephrine hydrochloride gel, applied three times a day, on the change from baseline to the end of study (8 weeks)in the faecal incontinence score (St Mark's) with passive faecal incontinence after ileo-anal pouch construction, compared with placebo. |
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| Study Phase | Phase III | ||||
| Study Type ICMJE | Interventional | ||||
| Study Design ICMJE | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Safety/Efficacy Study | ||||
| Condition ICMJE | Faecal Incontinence | ||||
| Intervention ICMJE | Drug: 10% Phenylephrine hydrochloride gel | ||||
| Study Arms / Comparison Groups | |||||
| Publications * | |||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Terminated | ||||
| Enrollment ICMJE | 0 | ||||
| Completion Date | November 2007 | ||||
| Primary Completion Date | |||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
NB: Seepage, leakage, soiling of faecal material is regarded as incontinence. Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United Kingdom | ||||
| Administrative Information | |||||
| NCT ID ICMJE | NCT00420797 | ||||
| Responsible Party | |||||
| Study ID Numbers ICMJE | P/PFI/01 | ||||
| Study Sponsor ICMJE | S.L.A. Pharma AG | ||||
| Collaborators ICMJE | |||||
| Investigators ICMJE |
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| Information Provided By | S.L.A. Pharma AG | ||||
| Verification Date | November 2007 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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