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ERAC Protocol in Elective Cesarean Surgery

NCT06672198 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 333

Last updated 2024-11-22

No results posted yet for this study

Summary

This descriptive prospective study was conducted between 01/12/2021-01/09/2022. The sample of the study consisted of 333 women who underwent elective cesarean section (CS). Nurse observation form, anesthesia follow-up form, patient file and verbal expressions of women were used to collect data. Number, percentage, mean and standard deviation were used as descriptive statistics.

Conditions

  • Cesrean Delivery
  • Enhanced Recovery After Surgery

Interventions

PROCEDURE

ERAC protocol

our study aimed to evaluate pre-peri-post operative practices in women who underwent elective cesarean section (CS) according to the ERAC protocol. In this context, this study aimed to describe the implementation status of the recommendations regarding the ERAC protocol in CS operations, to identify the missing aspects of the ERAC protocol and to raise awareness about its benefits.

Sponsors & Collaborators

  • Gonca Karatas Baran

    lead OTHER

Principal Investigators

  • gonca Karataş Baran, phd · Etlik Zübeyde Hanım Maternity and Women's Health Teaching and Research Hospital

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-12-01
Primary Completion
2021-12-01
Completion
2022-09-01

Countries

  • Turkey (Türkiye)

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 NCT06672198 on ClinicalTrials.gov