Effect of a cervical block on pain management after neck surgery
The Effect of Superficial Cervical Block Application on Postoperative Opioid Consumption in Patients Undergoing Anterior Cervical Discectomy Surgery
This study is testing if a special neck pain relief method can help patients after neck surgery use less opioid medication and feel better overall.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Medipol University Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06755736 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial evaluates how a superficial cervical block affects opioid consumption in patients undergoing anterior cervical discectomy surgery. The study aims to determine if this regional anesthesia technique can reduce the need for opioids post-surgery, thereby minimizing side effects like nausea and respiratory depression. Participants will be randomly assigned to receive either the cervical block or standard care, and their pain levels and opioid-related side effects will be monitored. The trial is conducted at Medipol Mega University Hospital, focusing on improving postoperative recovery and comfort.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-80 scheduled for anterior cervical discectomy surgery with ASA physical status I-III.
Not a fit: Patients with allergies to local anesthetics, pregnant women, or those with psychiatric or neurological disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce opioid use and its associated side effects for patients recovering from neck surgery.
How similar studies have performed: Previous studies have shown the effectiveness of superficial cervical blocks in other types of surgeries, suggesting potential success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients scheduled for anterior cervical discectomy surgery * aged between 18 and 80 years, * American Society of Anesthesiology (ASA) physical status I-III, scheduled for anterior cervical discectomy surgery will be included. Exclusion Criteria: * history of allergies, * allergic to local anesthetics, * pregnant women * psychiatric or neurological disorders
Where this trial is running
Istanbul
- Medipol University — Istanbul, Turkey (Recruiting)
Study contacts
- Study coordinator: Burak Ömür
- Email: bomur@medipol.edu.tr
- Phone: +905056215056
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.