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Sponsored by: |
S.L.A. Pharma AG |
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Information provided by: | S.L.A. Pharma AG |
ClinicalTrials.gov Identifier: | NCT00774722 |
The purpose of this study is to determine whether metronidazole 10% ointment , applied topically three times a day in and around the anus, on the reduction of pain following haemorrhoidectomy.
Condition | Intervention | Phase |
---|---|---|
Haemorrhoidectomy |
Drug: Metronidazole |
Phase II Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment |
Official Title: | Phase 2 Study Evaluation of Topical 10% Metronidazole Ointment for the Reduction of Pain After Haemorrhoidectomy |
Estimated Enrollment: | 40 |
Study Start Date: | September 2006 |
Study Completion Date: | March 2008 |
Primary Completion Date: | March 2008 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United Kingdom | |
St Thomas' Hospital, Lambeth Palace Road | |
London, United Kingdom, SE1 7EH | |
Royal Sussex County Hospital, Eastern Road, | |
Brighton, United Kingdom, BN2 5BE | |
North Middlesex University Hospital | |
London, United Kingdom, N18 1QX | |
Stepping Hill Hospital | |
Stockport, United Kingdom, SK2 7JE | |
St Marks Hospital | |
Harrow, United Kingdom, HA1 3UJ |
Study Director: | Christopher J Jordan, BSc | SLA Pharma |
Study ID Numbers: | MET/02, EudraCT Number 2005-001396-35 |
Study First Received: | October 16, 2008 |
Last Updated: | October 16, 2008 |
ClinicalTrials.gov Identifier: | NCT00774722 |
Health Authority: | United Kingdom: Medicines and Healthcare Products Regulatory Agency |
Metronidazole Pain |
Anti-Infective Agents Antiparasitic Agents Antiprotozoal Agents Radiation-Sensitizing Agents |
Therapeutic Uses Physiological Effects of Drugs Pharmacologic Actions |