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NCT06265571 Clinical Trial

Postoperative Pain in Shoulder Surgery

Pain, Postoperative Clinical Trial

Official title:
The Effect of Ultrasound-Guided Suprascapular Block Plus Low-dose Interscalen Brachial Plexus Block for Postoperative Pain in Shoulder Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06265571
Other study ID # EskisehirUO
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 15, 2020
Est. completion date July 15, 2021

Study information
Verified date February 2024
Source Eskisehir Osmangazi University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date July 15, 2021
Est. primary completion date June 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Other:
• perineural injection
perineural injection of local anesthestetic for postoperative pain management

Locations
Country Name City State
Turkey Ferda YAMAN Eskisehir Odunpazari

Sponsors (1)
Lead Sponsor Collaborator
Eskisehir Osmangazi University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary rescue analgesia postoperative pain score (VAS) > 4 required to rescue analgesia between 01.01.2019 and 01.03.2020
Primary difference between the analgesic methods between 01.01.2019 and 01.03.2020
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