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

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05235308

Enrollment

193

Registered

2022-02-11

Start date

2022-02-15

Completion date

2022-04-15

Last updated

2023-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Chronic

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.

Interventions

PROCEDUREPercutaneous adhesiolysis

Percutaneous adhesiolysis is a minimally invasive technique which involves the use of a spring-wound catheter, ideally placed in the ventrolateral aspect of the epidural space for the lysis of adhesions.

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* patients in whom percutaneous epidural lysis of adhesions was performed

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame	Description
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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026