Image

Enhanced Recovery Protocol Compliance and Quality of Recovery After Cesarean Delivery

Enhanced Recovery Protocol Compliance and Quality of Recovery After Cesarean Delivery

Recruiting
18 years and older
Female
Phase N/A
  • Technical (Original)
  • Simplified (AI rewritten)

Powered by AI

Overview

This prospective observational study will evaluate whether adherence to enhanced recovery after cesarean delivery protocols is associated with postoperative recovery quality in women undergoing elective cesarean delivery under spinal anesthesia. A total of 150 participants will be enrolled. Recovery quality will be assessed using the Turkish version of the Obstetric Quality of Recovery-10 questionnaire at 24 hours after surgery. Pain, opioid use, nausea, mobilization, oral intake, breastfeeding, and patient satisfaction will also be evaluated.

Eligibility

Inclusion Criteria:

  • Age 18 years or older
  • Scheduled for elective cesarean delivery
  • Planned spinal anesthesia
  • American Society of Anesthesiologists physical status II or III
  • Ability to read and understand Turkish
  • Provision of written informed consent

Exclusion Criteria:

  • Emergency cesarean delivery
  • General anesthesia or conversion from spinal to general anesthesia
  • Major obstetric hemorrhage
  • Requirement for postoperative intensive care
  • Chronic opioid use
  • Chronic pain syndrome
  • Severe psychiatric disease
  • Severe neurological disease
  • Inability to communicate
  • Cognitive impairment preventing completion of study questionnaires
  • Refusal to participate

Study details
    Cesarean Section
    Postoperative Recovery
    Postoperative Pain

NCT07790471

Bursa City Hospital

29 August 2026

Contact a study center
Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.