Clinical Trials Directory

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UnknownNCT00861562

Clinical Efficacy and Safety Evaluation of the Drug Imescard Compound Water Smartweed Pills

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Hospital de Clinicas de Porto Alegre · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to assess the clinical efficacy and safety of the drug Imescard water smartweed compound pills in the treatment of patients with chronic constipation and hemorrhoidal disease.

Detailed description

The Imescard compound water smartweed pills are currently registered in Brazil at the National Sanitary Surveillance Agency (ANVISA) as a laxative for the treatment of constipation, and as a supporting drug in hemorrhoid treatment. Though water smartweed (Polygonum hydropiperoides) has been used throughout the years as an antiinflammatory and in hemorrhoidal treatment, there are no reliable pharmacologic and clinical evidence that demonstrate its efficacy. The aim of this study was to assess the clinical efficacy and safety of the drug Imescard compound water smartweed pills in the treatment of chronic constipation and hemorrhoidal disease in a randomized, double-blind, crossover, placebo-controlled clinical trial. Volunteers underwent a clinical evaluation and laboratory exams at enrollment, and 56 patients met the inclusion criteria and agreed to sign the informed consent form. Participants were then randomized into two groups to receive either Imescard pills or placebo, identical in appearance, once at every 8 hours for five days, followed by a 10-day washout period, and then received the other intervention for another 5-day period. Followup visits were performed at day 1, 5, 15, and 19. At the beginning of each intervention period(days 1 and 15), patients were given diaries that included two questionnaires for each day of treatment, concerning constipation and hemorrhoidal symptoms, and received the intervention, unaware of its content. Colonic transit time was assessed at the end of each intervention period (days 5 and 19) through standard radiologic technique, and laboratory exams were taken three days later. Clinical evaluation and adverse effects assessment was performed at every visit by blinded investigator, and patients also fulfilled WHOQOL Brief, for life quality assessment.

Conditions

Interventions

TypeNameDescription
DRUGImescard water smartweed composed pills01 pill at every 8 hours for 5 days.
DRUGPlacebo01 pill at every 8 hours for 5 days, with the exact same appearance as the other intervention.

Timeline

Start date
2008-04-01
Primary completion
2008-10-01
Completion
2009-04-01
First posted
2009-03-13
Last updated
2009-03-13

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00861562. Inclusion in this directory is not an endorsement.