Comparison of continuous interscalene block and continuous suprascapular nerve block

Comparison of ultrasound-guided continuous interscalene brachial plexus block and arthroscopically-assisted continuous suprascapular nerve block in patients undergoing arthroscopic rotator cuff repair: a randomized controlled trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005500

Enrollment

100

Registered

2020-10-20

Start date

2020-12-22

Completion date

Unknown

Last updated

2022-09-20

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 : In interscalene group, ultrasound-guided single-shot interscalene block(superior trunk block) with 0.2% ropivacaine is performed and interscalene catheter is inserted for analgesia

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: * rotator cuff tear patient scheduled to undergo arthroscopic rotator cuff repair * American society of anesthesiologists physical status I/II/III

Exclusion criteria

Exclusion criteria: * patient who refuse to participate in this study * patient with moderate/severe pulmonary disease * patient with uncontrolled medical/psychological disease * patient with trauma history on ipsilateral side * patient with cervical disease, neuropathy, or myelopathy * patient who requires additional open surgery * patient who are contraindicated to NSAIDs, opioid, or ropivacaine * female who is pregnant or lactating * patient who are considered inappropriate by medical staffs due to other reasons

Design outcomes

Primary

Measure	Time frame
postoperative pain score	—

Secondary

Measure	Time frame
the change of diaphragmatic excursion measured by ultrasound;Forced expiratory volume 1;postoperative opioid consumption;postoperative complications including hematoma, dyspnea	—

Countries

Korea, Republic of

Contacts

Public ContactHa-Jung Kim

Asan Medical Center

alexakim06@gmail.com+82-2-3010-0338

Outcome results