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Compare Outcome of Enhanced Recovery After Cesarean Surgery and Conventional Care

NCT04530851 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2020-08-28

No results posted yet for this study

Summary

Research objective to compare outcome(Length of stay, pain score, opioid drug use, Bowel function and complication ) of ERAS protocol and conventional care in pregnant women after elective cesarean section in Rajavithi hospital.

Conditions

  • To Determine Whether ERAS Can Reduce Length of Stay in Pregnant Women After Cesarean Section

Interventions

PROCEDURE

ERAS

* Counseling * H2- antagonist and metroclopramide for prevent aspiration * Drink clear liquid until 2 hour before surgery * First generation cephalosporin in 60 minute before surgery * Clorhexidine for skin cleansing and Povidine for vaginal cleansing * Regional anesthesia * Keep warming * Blunt expansion of uterine incision * Do not peritoneal suture and subcuticular suture if less than 2 cm * Local wound anesthesia. * Paracetamol and NSAIDs for for pain control * Early remove catheter and ambulation * 5-HT3 antagonist for prevent nausea

Sponsors & Collaborators

  • Department of Medical Services Ministry of Public Health of Thailand

    lead OTHER_GOV

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-01-15
Primary Completion
2020-07-30
Completion
2020-07-30

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04530851 on ClinicalTrials.gov