Analgesic effect of periarticular cocktail injection after rotator cuff repair surgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400082001

Enrollment

Unknown

Registered

2024-03-18

Start date

2020-05-01

Completion date

Unknown

Last updated

2024-03-25

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

Conditions

Postoperative pain control for rotator cuff injury

Interventions

Cocktail Group:Cocktail

Analgesic pump Group:Postoperative oral analgesics

Eligibility

Sex/Gender

All

Age

57 Years to 68 Years

Inclusion criteria

Inclusion criteria: (1) Patients diagnosed with rotator cuff injury and undergoing arthroscopic rotator cuff repair; (2) Patients who are willing and able to provide written informed consent for their participation in the study; (3) Patients over 60 years old; (4) Patients with a body mass index less than 35kg/m2; (5) Patients with the ability to understand visual analog pain scales; (6) Patients without drug allergies; (7) Patients with ASA physical condition I-II.

Exclusion criteria

Exclusion criteria: (1) Patients with calcified tendinitis; (2) Patients with depression; (3) Anxiety patients; (4) Alcohol poisoning patients; (5) Patients with neurological disorders; (6) Patients with nodular avulsion fractures.

Design outcomes

Primary

Measure	Time frame
VAS;	—

Secondary

Measure	Time frame
Postoperative complications;	—

Countries

china

Contacts

Public ContactGan yudong

Qilu Hospital (Qingdao) of Shandong University

gasbzh-1981@163.com+86 185 6181 1225

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026