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C-Section sleep study: one in three new moms may struggle to rest

NCT ID NCT05757401

Knowledge-focused Sponsor: Mahidol University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study looked at how common poor sleep is after a C-section when spinal morphine is used for pain relief. Researchers followed 286 mothers and measured sleep quality, pain, nausea, and itching on the first night after surgery. The goal was to understand which factors lead to worse sleep, not to test a new treatment.

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

286 people

The number who actually took part.

Started

Mar 2023

Finished

May 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Who is studied

Parturients age \>,= 18 years old undergoing cesarean delivery

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, undergoing cesarean delivery * Receive spinal anesthesia with local anesthetic drug and intrathecal morphine * Understand Thai Exclusion Criteria: * Patients receive epidural block or nerve block * Patients require conversion to general anesthesia with any reasons * Patients require endotracheal intubation with any reasons * Patients admit to intensive care unit in postoperative period * Patients with the end of operation at the time 24.00-6.00 AM

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Conditions

The condition(s) this trial relates to.

insomnia Parasomnias sleep disorder

As listed by the trial registrant

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

Cesarean section complications Perioperative complication Sleep disturbance

Contacts and locations

Locations

  • Anesthesiology department, Siriraj hospital, Mahidol University

    Bangkok, 10700, Thailand

More trials for these conditions

Other studies related to the condition(s) this trial covers.