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The application effect of continuous suprascapular nerve block on the management of pain after rotator cuff repair

The application effect of continuous suprascapular nerve block on the management of pain after rotator cuff repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092061
Enrollment
Unknown
Registered
2024-11-08
Start date
2024-11-10
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Arthroscopic rotator cuff repair

Interventions

group PCSA:In PCNA group, suprascapular nerve puncture tube was inserted and controlled analgesia pump was connected. The formulated drug was 0.3% ropivacaine 300mI, the background infusion dose was s
group PCIA:In the PCIA group, intravenous controlled analgesia pump was connected after surgery, sufentanil citrate 2.5ug/kg, dexmetomidine 1ug/kg, remosetron 0.6mg,diluted with normal saline to 150ml

Sponsors

Guang 'an People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Age 45-60 years old; (2) Elective arthroscopic rotator cuff repair; (3)ASA physical status I–II; (4) Agree to anesthesia and postoperative analgesia plan; (5) Sign informed consent for anesthesia.

Exclusion criteria

Exclusion criteria: (1) Shoulder revision surgery; (2) Infection at the puncture site in the neck, deformity of the neck, history of neck surgery; (3) History of shoulder and arm movement and sensation abnormalities due to cervical spine disease or cerebral infarction; (4) Uncontrolled hypertension or diabetes; (5)Diabetic peripheral neuropathy;(6) Severe cardiopulmonary function impairment, liver or kidney dysfunction, or coagulation disorders; (7) Unconsciousness or mental abnormalities that prevent cooperation with the procedure; (8) Allergic to ultrasound coupling agents, local anesthetics, or opioid drugs; (9) Long-term oral administration of opioid analgesic drugs.

Design outcomes

Primary

MeasureTime frame
Pain intensity NRS score;

Secondary

MeasureTime frame
Inflammatory index detection;Adverse analgesic reaction;Evaluation of shoulder joint mobility function;

Countries

China

Contacts

Public ContactSulan Qin

Guang 'an People's Hospital

910037889@qq.com+86 135 5197 9552

Outcome results

None listed

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