Comparing pain relief methods for spinal surgery patients
The Effect of Erector Spinal Area (Esp) Block Applied Before or After Surgery on Postoperative Acute Pain and Quality of Recovery in Patients Undergoing Spinal Surgery
This study tests whether giving a pain relief injection before or after spinal surgery helps patients feel less pain and recover better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Aydin Adnan Menderes University Academic / other |
| Locations | 1 site (Aydın) |
| Trial ID | NCT06215053 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of the erector spinae plane (ESP) block for managing postoperative pain in spinal surgery patients. It compares two groups: one receiving the ESP block before surgery and the other after surgery. The study aims to determine which timing of the block provides better pain relief and reduces the risk of chronic pain. Patients will be monitored for pain levels and recovery outcomes postoperatively.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-75 undergoing elective spinal surgery with an ASA classification of I-III.
Not a fit: Patients requiring emergency surgery, those with chronic opioid use, or psychiatric disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for spinal surgery patients, enhancing recovery and reducing opioid use.
How similar studies have performed: Previous studies have shown promising results with the erector spinae block for postoperative pain management, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Spinal surgery performed under elective conditions 2. ASA I-III 3.18-75 years old Exclusion Criteria: 1. Rejection during registration 2. Request for dismissal from employment 3. Inability to give informed consent 4. Emergency surgery 5. Bleeding diathesis 6. Presence of contraindications to the LA agents used in this study 7. Chronic use of opioids 8. Psychiatric disorders 9. Presence of infection at the injection site
Where this trial is running
Aydın
- Ferdi Gülaştı — Aydın, Turkey (Recruiting)
Study contacts
- Study coordinator: ferdi Gülaştı
- Email: ferdigulasti@icloud.com
- Phone: +905054929650
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.