Comparison of the effect of ozone, corticosteroid and prolotherapy in coccydynia

Phase 3

Recruiting

• Conditions: Coccydynia.; Sacrococcygeal disorders, not elsewhere classified; M53.3

• Registration Number: IRCT20100827004641N17
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

Diagnosis of coccydynia
Age of 18-65 years
Pain score ranging from 1 to 10 in visual analogue scale

Exclusion Criteria

Tumors of the cauda equina
Pelvic surgery
Herniation of the lumbosacral disc

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity. Timepoint: Evaluating the visual analogue scale at the beginning of the study (before intervention) and 7 and 60 days after injection. Method of measurement: Visual analogue Scale.;Overall recovery rate. Timepoint: Evaluating the overall recovery rate at 7 and 60 days after injection. Method of measurement: Patient Global Impression of Improvement.