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Effect of Modified Cervical Nerve Root Block on Postoperative Rehabilitation Following Rotator Cuff Repair

Effect of Modified Cervical Nerve Root Block on Postoperative Rehabilitation Following Rotator Cuff Repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122196
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Postoperative pain

Interventions

Interscalene Brachial Plexus Block Group:The nerve block was performed using 20 mL of 0.375% ropivacaine.
Modified Cervical Nerve Root Block Group:The nerve block was performed using 6 mL of 0.375% ropivacaine
Modified Cervical Nerve Root Block Group:The nerve block was performed using 6 mL of 0.25% ropivacaine
Modified Cervical Nerve Root Block Group:The nerve block was performed using 6 mL of 0.5% ropivacaine

Sponsors

Gansu Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients meeting the diagnostic criteria and scheduled to undergo arthroscopic rotator cuff repair under general anesthesia; (2) Patients aged between 18 and 70 years old, with ASA grade I- II; (3) Patients who have signed the preoperative informed consent form and agreed to participate in this study.

Exclusion criteria

Exclusion criteria: (1) Patients who refuse to undergo nerve block procedures. (2) Patients with cognitive impairment (unable to understand pain assessment methods). (3) Patients with a history of diabetes mellitus. (4) Patients with a history of neurological deficit or neuropathy affecting the brachial plexus. (5) Hypersensitivity to any drugs used in the trial; presence of infection at the puncture site. (6) Severe cardiovascular disease, respiratory dysfunction, coagulation disorders, or neurological dysfunction

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale;—

Secondary

MeasureTime frame
Modified Bromage Scale;Procedure Time for Nerve Block;Onset and Duration of Sensory Block;Onset and Duration of Motor Block;Time to Resolution of Numbness in the Fingers on the Operated Side;Hemodynamic Stability;Intraoperative Arthroscopic Image Quality;Use of Rescue Analgesics within 24 Hours Postoperatively;24-Hour Patient and Surgeon Satisfaction Scores;Quality of Postoperative Recovery Score;—

Countries

China

Contacts

Public ContactZhang Xing

Gansu Provincial Hospital of Traditional Chinese Medicine

15285574946@163.com+86 152 8557 4946

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026