Coccydynia Clinical Trials

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Evaluation of the Effectiveness of Dextrose Prolotherapy on Pain Severity and Functional Status in Patients With Coccydynia: A Prospective Study

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Coccydynia is a musculoskeletal condition characterized by pain in the coccygeal region, particularly exacerbated by sitting, and is associated with impaired quality of life and functional limitation. Although various conservative and interventional treatment options are available, there remains a need for effective and safe alternative therapies, especially in treatment-resistant cases. Prolotherapy is a regenerative treatment modality that aims to reduce pain and improve function by stimulating tissue repair, particularly in ligamentous structures. While there is increasing evidence supporting its effectiveness in mechanical musculoskeletal pain conditions, the literature regarding its use in coccydynia is limited. The aim of this study is to evaluate the effect of dextrose prolotherapy on pain severity and functional status in patients diagnosed with coccydynia. This study is designed as a prospective, single-arm, open-label interventional study. Patients will receive 15% dextrose prolotherapy according to a standardized protocol. Pain severity will be assessed using the Visual Analog Scale (VAS), and functional status will be evaluated using the Dallas Pain Questionnaire before treatment and at 1 month after completion of the treatment. This study aims to provide more comprehensive data on the effectiveness and safety of prolotherapy in coccydynia and to contribute to the currently limited evidence in the literature.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Age between 18 and 75 years

• Pain persisting for ≥3 months and refractory to conservative treatment

• Coccydynia of mechanical or idiopathic origin

Locations
Other Locations
Turkey
Gaziosmanpasa Research and Education Hospital
RECRUITING
Istanbul
Contact Information
Primary
Merve Dikici Yagli, M.D
mervedikici1992@gmail.com
+905387192098
Backup
Yunus Emrah Kosut, M.D
kosutyunus@gmail.com
+905355540389
Time Frame
Start Date: 2026-01-15
Estimated Completion Date: 2026-06-15
Participants
Target number of participants: 30
Treatments
Experimental: Dextrose Prolotherapy
Participants will receive ultrasound-guided dextrose prolotherapy according to a standardized treatment protocol.
Related Therapeutic Areas
Sponsors
Leads: Gaziosmanpasa Research and Education Hospital

This content was sourced from clinicaltrials.gov