Predictive Factors on the Results of Epidural Adhesiolysis in Patient With Chronic Spinal Pain

Completed

• Conditions: Pain, Chronic

• Registration Number: NCT05235308
• Lead Sponsor: Diskapi Teaching and Research Hospital

Brief Summary

The primary aim of this exploratory study was to determine the demographic, clinical, and technical factors associated with treatment outcome, to create a better select treatment candidates.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-02-02
• Study First Submitted QC: 2022-02-02
• Study First Posted: 2022-02-11
• Study Start: 2022-02-15
• Primary Completion: 2022-03-15
• Study Completion: 2022-04-15
• Status Verified: 2023-08
• Last Update Submitted: 2023-08-13
• Last Update Posted: 2023-08-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 193

Inclusion Criteria

• patients in whom percutaneous epidural lysis of adhesions was performed

Exclusion Criteria

• nonadhesiolytic procedure
• lack of follow-up
• incomplete outcome data

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain intensity	baseline to 12 months post-procedure	The visual analog scale is a numerical scale from 0 to 10; with 0 representing no pain and 10 representing the worst pain imaginable.

Trial Locations

Locations (1)

Diskapi Yildirim Beyazit Training and Research Hospital; 🇹🇷 Ankara, Turkey