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Tailbone pain showdown: Hands-On therapy or nerve block?

NCT ID NCT07426497

Symptom relief Sponsor: Istanbul Medeniyet 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 24, 2026 · Updated 1 time

Summary

This study compares two treatments for chronic tailbone pain (coccydynia): osteopathic manual therapy (a hands-on approach) and a nerve block injection. Researchers will enroll 100 adults who have had tailbone pain for at least 3 months and have not gotten relief from other treatments. Participants will be randomly assigned to one of the two treatments, and their pain and ability to function will be measured at 3 weeks and 3 months. The goal is to find out which treatment works better to ease pain and improve daily life.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

105 people

The number who actually took part.

Started

Aug 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.

Ages

18 to 75 years

Sex

Anyone

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 18-75 years * Chronic coccygodynia ≥3 months * Baseline NRS ≥4 * ODI ≥20 * Failure of prior conservative treatment * Imaging excludes fracture, infection, or malignancy * Ability to provide written informed consent Exclusion Criteria: * Acute coccygodynia * Prior spinal or coccygeal surgery * Malignancy * Pelvic fracture * Pregnancy * Coagulation disorder * Severe psychiatric disease * Prior osteopathic manual therapy or ganglion impar block

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Conditions

The condition(s) this trial relates to.

Chronic Pain chronic pain syndrome coccygodynia

As listed by the trial registrant

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

Chronic pain Coccydynia Coccygodynia

Contacts and locations

Locations

  • Medicana Zincirlikuyu Hospital

    Istanbul, Sisli, 34394, Turkey (Türkiye)

More trials for these conditions

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