At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 164 enrolled
Drug / intervention
Probiotics +1 moredietary
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 Randomized Clinical Study of the Efficacy of a Formulation of Four Probiotics for the Prevention of Post-operative Complications in Patients Undergoing Colorectal Surgery
In Brief
A Phase 4 clinical trial evaluating Probiotics and Placebo for Postoperative Complications. Completed, enrolled 164 participants.
Detailed Summary
Based on the need of large-scale, trials to explore the use of probiotics to reduce post-operative complication rate, a randomized controlled trial is designed to investigate the impact of a probiotics treatment protocol on postoperative morbidity in an open elective colonic surgery cohort. The major objective is reduction of post-operative complications after 30 days.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPostoperative Complications
Countries--
CollaboratorsAristotle University Of Thessaloniki
Timeline
Phase 4CompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartApr 2013
Primary CompletionJul 2014
Study CompletionAug 2014
First PostedDec 2014
TodayJul 2026
First PostedDec 10, 2014
Enrollment StartApr 1, 2013
Primary CompletionJul 1, 2014
Study CompletionAug 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 11.6 years ago
Interventions
Probioticsdietary
Probiotics are prepared in capsule form
Placebodietary
Glucose powder