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Postoperative Pain in Shoulder Surgery

E

Eskisehir Osmangazi University

Status

Completed

Conditions

Pain, Postoperative

Treatments

Other: perineural injection

Study type

Observational

Funder types

Other

Identifiers

NCT06265571
EskisehirUO

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

arthroscopic shoulder surgery full data form

Exclusion criteria

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

Trial design

40 participants in 2 patient groups

GROUP I
Description:
Interscalene block (group I)15 ml of 0.5% bupivacaine was applied with a single injection to 12 of 18 patients,
Treatment:
Other: perineural injection
GROUP II
Description:
7.5 ml of interscalene and 7.5 ml of suprascapular block (GROUP II) were applied to 6 patients with posterior approach.
Treatment:
Other: perineural injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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