superior trunk block for shoulder surgery

The comparison of hemidiaphragmatic paralysis between continuous interscalene and continuous superior trunk block for shoulder surgery: a double-blinded, prospective randomized controlled trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005420

Enrollment

Registered

2020-09-23

Start date

2020-12-22

Completion date

Unknown

Last updated

2021-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : All patients are randomly assigned to two groups. In the experimental group, the patients were performed ultrasound guided superior trunk block. In the control group, the patients

Ropivacaine 10ml with epinephrine 1: 200000 (Naropin®, AstraZeneca, UK)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: American society of anesthesiology (ASA) physical status 1, 2, 3 Age: 19-80 yrs Patients undergoing arthroscopic shoulder surgery

Exclusion criteria

Exclusion criteria: Clinically significant coagulopathy Infection at the injection site Allergy to local anesthetics Severe cardiopulmonary disease(American society of anesthesiology (ASA) physical status =4) Body mass index > 35 Diabetic or other neuropathies Patients receiving opioids for chronic analgesic therapy Patients who have refused intravenous patient controlled analgesia (PCA) Inability to comprehend visual analogue scale (VAS) score and patient controlled analgesia (PCA) device Patient who does not want to receive superior trunk or interscalene block Patients who want to receive a superior trunk or interscalene block

Design outcomes

Primary

Measure	Time frame
Diaphragmatic paralysis;Assessment of pulmonary function	—

Secondary

Measure	Time frame
Amount of opioid consumption;postoperative pain	—

Countries

Korea, Republic of

Contacts

Public ContactYoungin Lee

The Catholic University of Korea, Daejeon St. Mary's Hospital

Outcome results