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
• Status: Completed
• 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
• 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

Related Conditions & MeSH terms

• Pain, Postoperative
• Shoulder Pain

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