At a glance
ClinicalIndex Comparison RecordPhase 2Completed
Drug / intervention
Polyethylene glycol 3350 NA bicarbonate NaCl KCl (Movicol) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Single Centre Study to Assess the Safety and Efficacy of Movicol in the Treatment of Faecal Impaction in Children Followed by a Double Blind, Randomised Phase to Compare the Safety and Efficacy of Movicol and Lactulose for Maintenance Therapy
In Brief
A Phase 2 clinical trial evaluating Polyethylene glycol 3350 NA bicarbonate NaCl KCl (Movicol) and Lactulose for Feces, Impacted. Completed, across 1 site.
Detailed Summary
This was a single centre study comprised of two stages (Parts I and II). Part I was a 9-day open label evaluation of Movicol administered to patients in hospital. This study evaluated the safety and efficacy of Movicol in treating faecal impaction. Movicol was administered over 3 - 7 days to achieve disimpaction.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsFeces, Impacted
CountriesUnited Kingdom
Collaborators--
Timeline
Phase 2CompletedFinished
200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartOct 2000
Study CompletionApr 2002
First PostedNov 2006
TodayJul 2026
First PostedNov 27, 2006
Enrollment StartOct 1, 2000
Study CompletionApr 1, 2002
TodayJul 2, 2026
Posted 19.6 years ago
Interventions
Polyethylene glycol 3350 NA bicarbonate NaCl KCl (Movicol)drug
Lactulosedrug