Effect of Interscalene and Suprascapular Nerve Block on Analgesia Consumption After Adhesive Capsulitis Surgery

Not Applicable

Completed

• Conditions: Shoulder Surgery
• Interventions: Procedure: suprascapular nerve block; Procedure: Group Control; Procedure: interscalene brachial plexus block

• Registration Number: NCT04769570
• Lead Sponsor: TC Erciyes University

Brief Summary

In this study, a combination of different types of blocks for adhesive capsulitis surgery, the investigators will investigate the impact on patient satisfaction and analgesic consumption after surgery.

Detailed Description

General anesthesia will be performed in all patients for arthroscopic adhesive capsulitis shoulder surgeries. In the first group of patients (Group IPSB), interscalene brachial plexus block will be applied 30 minutes before surgery, while interscalene brachial plexus block and suprascapular nerve block (SSNB) administration to the second group patients (Group SSNB) before surgery. Patients in the third group (Group C) will be considered the control group and no block will be performed. Patient-controlled analgesia (PCA) with morphine will be used in all three groups for postoperative analgesia. Preoperative hemodynamic data of patients, postoperative pain scores (VAS), morphine consumption, patient satisfaction score, requirement of additional analgesia and observed side effects were recorded. Consumption of analgesia 24 hours after surgery and patient satisfaction will be evaluated.

Study Timeline

• Study First Submitted: 2021-02-21
• Study First Submitted QC: 2021-02-21
• Study Start: 2021-02-22
• Study First Posted: 2021-02-24
• Primary Completion: 2021-12-29
• Study Completion: 2021-12-31
• Status Verified: 2022-07
• Last Update Submitted: 2022-07-28
• Last Update Posted: 2022-07-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

• ASA I- ASA II Patients

Exclusion Criteria

• history of allergy to the study medication
• refusal to participate

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Group SSNB	suprascapular nerve block	In the second group of patients, ultrasound-guided interscalene brachial plexus block and suprascapular nerve block will be applied 30 minutes before surgery.
Group Control	Group Control	Patients in the third group (Group C), will be considered the control group and no block will be performed.
Group IPSB	interscalene brachial plexus block	In the first group of patients (Group IPSB), ultrasound-guided interscalene brachial plexus block will be applied 30 minutes before surgery.

Primary Outcome Measures

Name	Time	Method
Verbal Analogue Scores	24 hours after surgery	A research assistant, blinded to the group allocation, interviewed patients and collected data in the 24 hours postoperative period.Verbal Analog Pain Score value will be the lowest 0 and the highest 10. At the highest value, the patient's pain is at its maximum. and whether higher scores mean worse outcome.
opioid consumption	24 hours after surgery	In the recovery room all patients will be given a patient-controlled analgesia device containing morphine and 24 hours postoperative period will be recorded.

Secondary Outcome Measures

Name	Time	Method
Complications of the procedures	During the blocks and 24 hours after surgery	The complications of the intervations will be recorded

Trial Locations

Locations (1)

Sibel Seçkin Pehlivan; 🇹🇷 Kayseri, Talas, Turkey