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Efficacy of the enhanced recovery after surgery (ERAS) protocol following elective cesarean section, a single-center randomized controlled trial

Efficacy of the enhanced recovery after surgery (ERAS) protocol following elective cesarean section, a single-center randomized controlled trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210705001
Enrollment
48
Registered
2021-07-05
Start date
2020-05-05
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

compare the efficacy of postoperative recovery among pregnant women scheduled for caesarean section and receiving enhanced recovery after surgery protocol (ERAS) compared with the 24 hour postoperative control group using the Thai version of the Quality of recovery questionnaire ( QoR-35). ERAS, QoR-35

Interventions

-Explain the indications for the procedure, the preparation before surgery, the possible complications, and the recovery time after surgery -Giving patients water to drink A solution containing 50 gm
Experimental Other
ERAS protocol

Sponsors

Srinakharinwirot University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: i) Women aged 20-40 years ii) Singleton pregnancy without severe obstetric (Gestational diabetic mellitus) or severe medical complications such as kidney disease, asthma, heart disease, pregestational diabetic mellitus

Exclusion criteria

Exclusion criteria: i) subsequently had postpartum hemorrhage, ii) Received (or be converted to) general anesthesia, iii) Underwent emergency cesarean section, or iv) demonstrated unstable post-operative condition (shock, anaphylaxis, respiratory distress) iv) Contraindication to use cefazolin, NSAIDs, metoclopramide, v) Cannot read Thai questionnaire, vi) Refuse to joint research

Design outcomes

Primary

MeasureTime frame
Quality of recovery 24 hours postoperative QoR-35 scores

Secondary

MeasureTime frame
24 hours postoperative pain score 24 hours postoperative Visual analogue scale,Postoperative complication 72 hours postoperative complication of surgery and puerperium

Countries

Thailand

Contacts

Public ContactNutchar Klangprapan

HRH Princess Maha Chakri Sirindhorn Medical Center, Srinakharinwirot University hospital

msmcmd058@gmail.com0861114803

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026