costoclavicular block

The comparison of hemidiaphragmatic paralysis between interscalene and costoclavicular block for shoulder surgery: a prospective randomized controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002376

Enrollment

Registered

2017-07-14

Start date

2017-08-10

Completion date

Unknown

Last updated

2025-04-07

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 costoclavicular block. In the control group, the patients

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: American society of anesthesiology (ASA) physical status 1, 2, 3 Age: 19-80 yrs Patients undergoing shoulder arthroscopic 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 costoclavicular or interscalene block Patients who want to receive a costoclavicular 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 ContactSeunguk Bang

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

seungukb@naver.com+82-42-220-9046

Outcome results