Clinical Trials Directory

Trials / Completed

CompletedNCT03477266

Mouth Dissolving Mosapride Tables Enhance Post Cesarean Gut Recovery

Effectiveness of Mouth Dissolving Mosapride Tablets on Enhancing Gut Recovery After Cesarean Section: Randomized Double-blind, Placebo-controlled Clinical Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
400 (actual)
Sponsor
Benha University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Giving women one day before and immediately after cesarean section a mouthly dissolving mosapride tablets 2every every 8 hours for maximum of 5 days ,or getting recovered gastrointestinal functions And assess preoperative gastrointestinal functions

Detailed description

Uncomplicated post cesarean women one day before and immediately after elective cesarean receive 2 mouthly dissolving mosapride tablets every 8 hours maximum for 5 days and clinical care giver follow the woman's gastrointestinal functions, including intraoperative and postoperative nausea vomiting, passing flatus, hearing intestinal sounds, passing stools, occurring of paralytic ileus, length of the hospital stay

Conditions

Interventions

TypeNameDescription
DRUGMosaprideIntake mouthly dissolving mosapride tablets in immediate post cesarean section
DRUGPlacebo Oral TabletDummy identical tablets to mouthly dissolving mosapride tablets

Timeline

Start date
2018-04-01
Primary completion
2018-06-01
Completion
2018-08-01
First posted
2018-03-26
Last updated
2018-08-14

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03477266. Inclusion in this directory is not an endorsement.