Effect of Shoulder Injection for Postoperative Analgesia in Shoulder Surgery

Effect of Multimodal Shoulder Injection for Postoperative Analgesia in Arthroscopic Rotator Cuff Repair under Interscalene Nerve Block - A Prospective Randomized Controlled Trial -

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008865

Enrollment

Registered

2023-10-12

Start date

2023-03-23

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

None listed

Interventions

Drug, Procedure/Surgery : For patients assigned to the injection group, modified Ranawart injection was administered after arthroscopic rotator cuff repair. Prepare two 50 ml syringes by mixing physio

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Among patients with full-thickness rotator cuff tears in the shoulder joint, patients undergoing arthroscopic rotator cuff repair through interscalene block, Patients who agreed to participate in this study

Exclusion criteria

Exclusion criteria: - Extensive rotator cuff tear - Elderly patients over 75 years of age - Patients for whom local nerve anesthesia is contraindicated due to blood clotting disorders, etc. - Patients undergoing revision surgery due to primary surgery failure - Patients with a history of ipsilateral shoulder surgery - Patients with neurological lesions of the ipsilateral shoulder - Patients who discontinued IV-PCA due to side effects within 48 hours after surgery

Design outcomes

Primary

Measure	Time frame
pain after surgery	—

Secondary

Measure	Time frame
Fentanyl dosage, number of administrations of pethidine hydrochloride 25 mg within 48 hours of surgery	—

Countries

Korea, Republic of

Contacts

Public ContactYoung Dae Jeon

Ulsan Univeristy Hospital

ydjeon84@gmail.com+82-52-250-7120

Outcome results