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Can simple recovery checklists after cesarean boost patient well-being?

NCT ID NCT07790471

Knowledge-focused Sponsor: Bursa City Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time

Summary

This study looks at whether following a set of enhanced recovery steps before, during, and after a planned cesarean delivery is linked to better recovery quality. Researchers will track 150 women having elective cesareans under spinal anesthesia, scoring how many protocol steps each woman receives. The day after surgery, women answer a questionnaire about their recovery, and the team also records pain, nausea, mobility, and breastfeeding. The goal is to see if higher adherence to the protocol matches better recovery outcomes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Enhanced recovery after cesarean delivery protocol (standard care components, no extra intervention)
What this could lead to
If higher adherence improves recovery, hospitals could adopt these steps more consistently to help women feel better and recover faster after cesarean delivery.
What could go wrong
This is an observational study, so it can show a link but not prove cause. Results may not apply to emergency cesareans or women with complications.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 150 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2026

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adult pregnant women aged 18 years or older undergoing elective cesarean delivery under spinal anesthesia at Bursa City Hospital, Türkiye. Eligible participants will have American Society of Anesthesiologists physical status II or III and will be enrolled consecutively during the study period.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cesarean section Postoperative pain Postoperative recovery

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Bursa City Hospital

    RECRUITING

    Bursa, Nilüfer, 16110, Turkey (Türkiye)

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