Trials / Completed
CompletedNCT04343937
Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 30 (actual)
- Sponsor
- Erzincan University · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
This retrospective study included 30 patients scheduled for lumbar herniectomy under general anesthesia. The patients were randomized to receive either retrolaminar block or intravenous analgesia treatment.Numeric Pain Rating Scale (NPRS) was used to measure the pain intensity of patients in postoperative period. Postoperative analgesic requirements were recorded to asses effectiveness of regional anesthesia.Opiod and NSAİD as rescue medication were recorded postoperatively.
Detailed description
This retrospective study included 30 patients scheduled for lumbar herniectomy under general anesthesia. The patients were randomized to receive either RLB or intravenous analgesia treatment. All patients were routinely monitored and their heart rate, blood pressure and pulse oxymetry recorded during the anesthesia. Numeric Pain Rating Scale (NPRS) scores evaluated at 2, 8, 12, 24 and 48 h after the surgery. Opiod and NSAİD as rescue medication were recorded postoperatively
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | retrolaminar block | local anesthetic injection on the between the lamina of the vertebra and the paraspinous muscle |
Timeline
- Start date
- 2020-04-15
- Primary completion
- 2020-06-15
- Completion
- 2020-06-15
- First posted
- 2020-04-14
- Last updated
- 2020-09-21
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT04343937. Inclusion in this directory is not an endorsement.