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Modified cocktail formula for analgesia after arthroscopic rotator cuff repair and early functional rehabilitation after arthroscopic rotator cuff repair

Modified cocktail formula for analgesia after arthroscopic rotator cuff repair and early functional rehabilitation after arthroscopic rotator cuff repair: a multicenter, prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084489
Enrollment
Unknown
Registered
2024-05-17
Start date
2024-05-30
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

rotator cuff injury

Interventions

cocktail group:the cocktail was injected into the shoulder joint cavity
control group:the saline was injected into the shoulder joint cavity

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were patients aged 18 years or older with a diagnosis of a full rotator cuff tear confirmed by clinical and imaging criteria. Patients with a tear of less than 4 centimeters in one or more tendons. All patients had persistent pain and dysfunction for at least six months and failed conservative treatment for six months.

Exclusion criteria

Exclusion criteria: Exclusion criteria include: severe osteoarthritis or articular cartilage disease of the shoulder joint; glenoid labral injury or Bankart injury; history of shoulder surgery; severe arthritic trauma, infection, or osteonecrosis of the shoulder; partial rotator cuff tear; inability to cooperate with treatment due to speech impairment; neuromuscular dysfunction affecting upper extremity function; history of opioid overdose; history of excessive alcohol use; mental illness; and comorbid thrombotic events (myocardial infarction, cerebrovascular accident, deep vein thrombosis, or pulmonary embolism).

Design outcomes

Primary

MeasureTime frame
Postoperative remedial morphine hydrochloride dosage;

Secondary

MeasureTime frame
Time to first use of morphine for remedial analgesia;VAS score;time of discharge;American shoulder and elbow surgeons, ASES;erythrocyte sedimentation rate;C-reactive protein;Interleukin 6;

Countries

China

Contacts

Public ContactLi Bohua

General Hospital of Ningxia Medical University

lbh0807@163.com+86 153 7954 5839

Outcome results

None listed

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