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OpenTrials
Completed

NCT Number: NCT05157022

Comparative Effects of Radial and Focused Extracorporeal Shock-wave Therapies in Coccydynia

Comparison of the efficacy of coccydynia treatment with two different probes of the ESWT device

Completed

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yüzüncü Yıl Üniversitesi Tıp Fakültesi

Van, 65080, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of coccydynia by clinical examination and X-ray imaging.
  • be aged ≥18 at the time of diagnosis
  • be give informed consent

Exclusion criteria

  • Malignancy
  • Those who have received ESWT treatment before
  • Pediatric patients
  • Patients with infection.

Treatment and study plan

ESWT

Device

Extracorporeal Shock-wave Therapy

Primary outcomes

  1. Visual Analogue Scale

    Time frame: 1 minute

    pain evaluation, higher scores mean worse outcome.

  2. Oswestry Low Back Pain Disability Questionnaire

    Time frame: 5 minutes

    higher scores mean better outcome.

Sponsors and collaborators

Lead sponsor

Yuzuncu Yil University

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Dec 14, 2021
Registry last updated
Apr 28, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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