At a glance
ClinicalIndex Comparison RecordN/ACompleted· 193 enrolled
Drug / intervention
Percutaneous adhesiolysisprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Predictive Factors on the Results of Percutaneous Epidural Adhesiolysis in Patient With Chronic Spinal Pain
In Brief
An observational study evaluating Percutaneous adhesiolysis for Pain, Chronic. Completed, enrolled 193 participants across 1 site.
Detailed 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.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPain, Chronic
CountriesTurkey (Türkiye)
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
First PostedFeb 2022
Enrollment StartFeb 2022
Primary CompletionMar 2022
Study CompletionApr 2022
TodayJul 2026
First PostedFeb 11, 2022
Enrollment StartFeb 15, 2022
Primary CompletionMar 15, 2022
Study CompletionApr 15, 2022
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 4.4 years ago
Interventions
Percutaneous adhesiolysisprocedure
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.