Pain, Chronic Clinical Trial
Official title:
Predictive Factors on the Results of Percutaneous Epidural Adhesiolysis in Patient With Chronic Spinal Pain
| NCT number | NCT05235308 |
| Other study ID # | 127/22 |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | February 15, 2022 |
| Est. completion date | April 15, 2022 |
| Verified date | August 2023 |
| Source | Diskapi Teaching and Research Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
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.
| Status | Completed |
| Enrollment | 193 |
| Est. completion date | April 15, 2022 |
| Est. primary completion date | March 15, 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - patients in whom percutaneous epidural lysis of adhesions was performed Exclusion Criteria: - nonadhesiolytic procedure - lack of follow-up - incomplete outcome data |
| Country | Name | City | State |
|---|---|---|---|
| Turkey | Diskapi Yildirim Beyazit Training and Research Hospital | Ankara |
| Lead Sponsor | Collaborator |
|---|---|
| Diskapi Teaching and Research Hospital |
Turkey,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | pain intensity | The visual analog scale is a numerical scale from 0 to 10; with 0 representing no pain and 10 representing the worst pain imaginable. | baseline to 12 months post-procedure |
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