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New questionnaire may help assess tailbone pain in new mothers

NCT ID NCT07089147

Knowledge-focused Sponsor: KTO Karatay 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This completed study of 292 women looked at tailbone pain (coccydynia) after childbirth. Researchers used the Paris Questionnaire to measure pain and compared it with quality-of-life and functional scores. The goal was to see if this simple questionnaire could help doctors better understand and assess postpartum tailbone pain.

What this could mean

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

What this could lead to
If successful, this could lead to better ways to measure and understand tailbone pain after childbirth, improving how doctors assess and manage the condition.
What could go wrong
This is an observational study using questionnaires, not a treatment trial. It cannot prove any therapy works, and results may not apply to all women with postpartum tailbone pain.

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

292 people

The number who actually took part.

Started

Aug 2025

Finished

Oct 2025

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

Females who have not previously received any treatment for coccydynia, who are within a maximum of 2 years postpartum, and who voluntarily agree to participate in the study will be included.

Ages

18 to 65 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 between 18 and 65 years of age * Having not received any previous treatment for coccydynia * Having given birth within the last 2 years at most Exclusion Criteria: * Those who have undergone surgical intervention on their spine * Those with a history of malignancy * Those with rectal or gynecological diseases

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Conditions

The condition(s) this trial relates to.

coccygodynia puerperal disorder

As listed by the trial registrant

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

Coccydynia Postpartum

Contacts and locations

Locations

  • Kto Karatay University

    Konya, Karatay, 42030, Turkey (Türkiye)

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