Skip to main content
MedPathMedPath Home
Clinical Trials/TCTR20181202001
TCTR20181202001
Enrolling By Invitation
Phase 2

A Randomized Controlled Trial Comparing Early versus Conventional Oral Feeding after Cesarean Section under Regional Anesthesia on Bowel Function

Department of obstetric and gynecology, faculty of medicine,Ramathibodi hospital, Mahidol university0 sites148 target enrollmentDecember 2, 2018
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsEarly oral feedingConventional oral feedingbowel functioncesarean sectiontime to passing flatustime to passing stooltime to ambulationtime to lactationsatisfaction levelEarly oral feedingConventional oral feedingbowel functioncesarean sectiontime to passing flatustime to passing stooltime to ambulationtime to lactationsatisfaction level

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Early oral feedingConventional oral feedingbowel functioncesarean sectiontime to passing flatustime to passing stooltime to ambulationtime to lactationsatisfaction level
Sponsor
Department of obstetric and gynecology, faculty of medicine,Ramathibodi hospital, Mahidol university
Enrollment
148
Status
Enrolling By Invitation
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 2, 2018
End Date
December 31, 2018
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Department of obstetric and gynecology, faculty of medicine,Ramathibodi hospital, Mahidol university

Eligibility Criteria

Inclusion Criteria

  • •â€¢ Singleton pregnancy women who underwent cesarean
  • •section under regional anesthesia
  • •â€¢ After giving research information, desire to join the
  • •â€¢ No intraoperative and postoperative complications
  • •â€ GI injury
  • •â€ GU injury
  • •â€¢ No another surgery except tubal ligation
  • •â€¢ No history of GI surgery or underlying disease that
  • •effects consuming

Exclusion Criteria

  • •â€¢ Need to delay postoperative oral feeding
  • •\> 6\-12 hr
  • •â€ Severe preeclampsia (postpartum)
  • •â€ Postparturm hemorrhage (\> 6\-12 hr postpartum)

Outcomes

Primary Outcomes

Not specified

Similar Trials

Not yet recruiting
Phase 2
Comparison of early versus late removal of urinary catheter after surgery for cervical cancer
CTRI/2018/11/016299FLUID RESEARCH GRANT
Not yet recruiting
Not Applicable
A randomized, controlled trial of early versus late initiation of peritoneal dialysisend stage renal disease patientsESRDPeritoneal dialysisglomerular filtration rateinitiation of dialysis
TCTR20140814001Health System Research Institute (HSRI), Thailand400
Completed
Not Applicable
A comparison of the overall pain scores post caesarean section, when initial intraoperative analgesia is given intravenously (IV) versus per rectum (PR).
ACTRN12614001144606Darren Lowen100
Not yet recruiting
Phase 4
A comparison of the overall pain scores post elective caesarean section, when initial intraoperative analgesia is given intravenously (IV) versus per rectum (PR).Analgesic requirements post elective caesarean sectionAnaesthesiology - Pain managementReproductive Health and Childbirth - Childbirth and postnatal care
ACTRN12615000997550Darren Lowen200
Recruiting
Not Applicable
Study to compare the difference between the outcomes of liver transplant between usage of synthetic graft(PTFE) vs native tissue graft(portal vein)
CTRI/2018/11/016315Amrita Institute of Medical Sciences Research Centre