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Pain awareness before surgery may shape recovery, study finds

NCT ID NCT07065188

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

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how being very aware of pain before vaginal surgery affects pain, bladder and bowel function, and sexual life after surgery. Researchers tracked 77 women before and after their operation using questionnaires. The goal was to see if pain hypervigilance leads to worse outcomes, helping doctors better prepare patients for surgery.

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

77 people

The number who actually took part.

Started

Oct 2025

Finished

Feb 2026

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

Have undergone vaginal surgery

Ages

18 to 40 years

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: * Being aged 18-40. * Being able to read and write Turkish. * Have undergone vaginal surgery. Exclusion Criteria: * Presence of any confounding condition in post-operative pain severity (patients with a history of chronic pelvic pain and/or endometriosis or pelvic inflammatory disease), * Having conditions in which sexual activity is contraindicated and should be restricted (genital infection, etc.), * Vulvovaginal infection, * Having a neurological disease, * Having visual, auditory, and cognitive problems that may prevent participation in the study.

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As listed by the trial registrant

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

Vaginal surgery

Contacts and locations

Locations

  • Acıbadem University

    Istanbul, 34752, Turkey (Türkiye)

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