Comparison of the Postoperative Analgesic Efficacy of SPSIPB and ESPB in Anterior Cervical Discectomy

Not Applicable

Recruiting

• Conditions: Anterior Cervical Discectomy; Peripheral Nerve Block; Pain Management

• Registration Number: NCT06639022
• Lead Sponsor: Ankara Etlik City Hospital

Brief Summary

Anterior cervical discectomy is an operation performed for complaints of pain, numbness or loss of strength due to cervical disc disease. With this operation, pressure due to herniation on the upper neck area, spinal cord or nerve roots is relieved. It is performed by microscopic method from the front of the neck.

Nerve blocks reduces opioid consumption in the postoperative period by providing better pain control and therefore has advantages such as fewer side effects and less risk of pulmonary and cardiac complications.

In this study; it was aimed to compare the analgesic effectiveness of serratus posterior superior intercostal plane block and erector spinae plane block, with each other and with the control group in the postoperative period in patients who underwent anterior cervical discectomy.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-10-10
• Study First Submitted QC: 2024-10-10
• Study Start: 2024-10-15
• Study First Posted: 2024-10-15
• Status Verified: 2024-11
• Last Update Submitted: 2024-11-04
• Last Update Posted: 2024-11-05
• Primary Completion: 2025-10-10
• Study Completion: 2025-11-20

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 85

Inclusion Criteria

• Patients aged 18-80 years
• American Society of Anesthesiologists (ASA) score I-II-III
• Body Mass Index (BMI) between 18-30 kg/m2

Exclusion Criteria

• Patients under 18 and over 80 years of age
• ASA score IV and above
• Patients with a history of bleeding diathesis
• BMI below 18 or above 30 kg/m2

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Pain Scores	On the operation day	Pain will be assessed at rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). Pain assessment will be done at 0st, 1st, 2nd,4th, 12th, and 24th hours after surgery.

Secondary Outcome Measures

Name	Time	Method
Intraoperative remifentanil consumption Intraoperative opioid consumption	Intraoperative period	Remifentanil consumption for intraoperative period will be recorded
Postoperative Tramadol Consumption	On the operation day	Tramadol consumption for 24 hours will be recorded

Trial Locations

Locations (1)

Ankara Etlik City Hospital; 🇹🇷 Altındağ, Ankara, Turkey

Ankara Etlik City Hospital

🇹🇷Altındağ, Ankara, Turkey

Atakan Sezgi, M.D.

Contact

00905323327000

kansezgi@gmail.com

Musa Zengin, Associate Professor

Contact

00905307716235

musazengin@gmail.com