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
| Type | Name | Description |
|---|---|---|
| DRUG | Mosapride | Intake mouthly dissolving mosapride tablets in immediate post cesarean section |
| DRUG | Placebo Oral Tablet | Dummy 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.