Skip to content

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
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03477266
Enrollment
400
Registered
2018-03-26
Start date
2018-04-01
Completion date
2018-08-01
Last updated
2018-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prevention of Postoperative Ileus

Keywords

Postoperative ileus, mosapride, mouth dissolving tablets, Intraoperative vomiting

Brief 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

Interventions

Intake mouthly dissolving mosapride tablets in immediate post cesarean section

DRUGPlacebo Oral Tablet

Dummy identical tablets to mouthly dissolving mosapride tablets

Sponsors

Benha University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Masking description

Color coded active tablets backed in red while identical dummy tablets coded in blue,both tablets are physically identical and usually no anticipated noticed side effects from mosapride

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* all women undergoing elective cesarean section

Exclusion criteria

* prior abdominal surgery, abdominal adhesion, chronic constipation, allergy to mosapride

Design outcomes

Primary

MeasureTime frameDescription
Time of first flatus96 hours postoperativeClinical

Secondary

MeasureTime frameDescription
Paralytic ileus incidence and its severity7daysClinical
Toleration of fluids and solids intake2 weeks postoperativeClinical
Incidence of intraoperative and postoperative nausea and vomitingIntraoperative and 2 weeks postoperativeClinical
First defecation2 weeks postoperativeClinical

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026