Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT07426497

Osteopathic Manual Therapy vs Ganglion Impar Block for Chronic Coccydynia

Led by Istanbul Medeniyet University · Updated on 2026-02-24

100

Participants Needed

1

Research Sites

24 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic coccydynia is a condition characterized by persistent pain in the coccyx region that can significantly impair sitting tolerance, daily activities, and quality of life. Various conservative and interventional treatment options have been described, including manual therapy techniques and ganglion impar block. However, the comparative effectiveness of these approaches remains unclear. The aim of this randomized controlled study is to compare the effects of osteopathic manual therapy and ganglion impar block on pain intensity and functional disability in patients with chronic coccydynia. Participants will be randomly assigned to one of the two treatment groups. Pain severity will be assessed using the Numeric Rating Scale (NRS), and functional status will be evaluated with the Oswestry Disability Index (ODI) at baseline, week 3, and month 3. The results of this study are expected to provide evidence regarding the relative effectiveness of these two commonly used treatment methods and to guide clinicians in selecting appropriate management strategies for patients with chronic coccydynia.

CONDITIONS

Official Title

Osteopathic Manual Therapy vs Ganglion Impar Block for Chronic Coccydynia

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-75 years
  • Chronic coccygodynia lasting 3 months or more
  • Baseline Numeric Rating Scale (NRS) pain score of 4 or higher
  • Oswestry Disability Index (ODI) score of 20 or higher
  • Failure of prior conservative treatment
  • Imaging excludes fracture, infection, or malignancy
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Acute coccygodynia
  • Prior spinal or coccygeal surgery
  • Malignancy
  • Pelvic fracture
  • Pregnancy
  • Coagulation disorder
  • Severe psychiatric disease
  • Prior osteopathic manual therapy or ganglion impar block

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medicana Zincirlikuyu Hospital

Istanbul, Sisli, Turkey (Türkiye), 34394

Actively Recruiting

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Research Team

M

mert sancar, MD

CONTACT

E

Ekim Can Ozturk, Md

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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