Trials / Completed
CompletedNCT05244031
Intraoperative Placement of Superficial Erector Spinae Plane Block; A New Approach in Spine Surgery
Intraoperative Placement of Superficial Erector Spinae Plane Block in Spine Surgery; An Effective Approach at Enhanced Recovery After Spine Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 46 (actual)
- Sponsor
- Bakirkoy Dr. Sadi Konuk Research and Training Hospital · Other Government
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Major spine surgery causes severe postoperative pain. The primary objective of this randomized controlled study is to compare the effect of ultrasound (US)-guided superficial erector spinae plane (ESP) block on 48-hour postoperative cumulative opioid requirements with standard (opioid-based) analgesia.
Detailed description
46 patients (ASA I-II-III) between 18 and 65 years of age, who were to undergo spine surgery, were randomized and divided into two groups. (23 patients in each of the control and superficial ESP groups). Superficial ESP block was performed for SESP group and standard (opioid-based) analgesia performed in the control group. Postoperative analgesia was provided by intravenous morphine infusion using a patient-controlled analgesia device. Postoperative numeric rating scale values were the primary outcome measure. 24-hour total morphine consumption was secondary outcome measure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | superficial erector spina plane block | The investigators performed superficial erector spina plane block to that patient group for postoperative analgesia |
| PROCEDURE | Standard (opioid-based) analgesia | The investigators performed intravenous opioid infusion with PCA to that patient group for postoperative analgesia |
Timeline
- Start date
- 2021-05-10
- Primary completion
- 2022-02-07
- Completion
- 2022-02-07
- First posted
- 2022-02-17
- Last updated
- 2022-03-03
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT05244031. Inclusion in this directory is not an endorsement.