Postoperative Pain in Shoulder Surgery

Completed

• Conditions: Pain, Postoperative

• Registration Number: NCT06265571
• Lead Sponsor: Eskisehir Osmangazi University

Brief Summary

After the approval of the ethics committee, the files of the patients who underwent arthroscopic shoulder surgery between 01.01.2019 and 01.03.2020 were evaluated retrospectively.

Data were recorded including age, gender, duration of anesthesia, duration of surgery, postoperative analgesia consumption, complications such as respiratory distress due to hemidiaphragmatic paralysis and complications such as hematoma and nerve damage due to block intervention.

Detailed Description

Patients who underwent arthroscopic shoulder surgery and underwent USG-guided interscalene block and concomitant suprascapular block were included in the study. We tried to determine whether there is a difference between different dose regimens in order to determine the effective analgesic dose and minimize the side effects of dose-dependent interscalene block applications.

Study Timeline

• Study Start: 2020-11-15
• Primary Completion: 2021-06-15
• Study Completion: 2021-07-15
• Study First Submitted: 2023-09-11
• Status Verified: 2024-02
• Study First Submitted QC: 2024-02-16
• Last Update Submitted: 2024-02-16
• Study First Posted: 2024-02-20
• Last Update Posted: 2024-02-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

arthroscopic shoulder surgery full data form

Exclusion Criteria

chronic obstructive lung disease chronic opoid consumption missing data from the postoperative pain form

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
rescue analgesia	between 01.01.2019 and 01.03.2020	postoperative pain score (VAS) \> 4 required to rescue analgesia
difference between the analgesic methods	between 01.01.2019 and 01.03.2020

Trial Locations

Locations (1)

Ferda YAMAN; 🇹🇷 Eskişehir, Odunpazarı, Turkey