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Effects of Ultrasound-Guided Superior Trunk Block with Different Ropivacaine Volumes on Hemidiaphragmatic Paralysis and Analgesic Efficacy in Patients Undergoing Arthroscopic Rotator Cuff Repair: A Prospective Randomized Controlled Trial

Effects of Ultrasound-Guided Superior Trunk Block with Different Ropivacaine Volumes on Hemidiaphragmatic Paralysis and Analgesic Efficacy in Patients Undergoing Arthroscopic Rotator Cuff Repair: A Prospective Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088722
Enrollment
Unknown
Registered
2024-08-26
Start date
2024-09-23
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Diaphragmatic paralysis

Interventions

Low dose group:Under ultrasound guidance, 5 ml of 0.4% ropivacaine was injected around the superior trunk of the brachial plexus.
Medium dose group:Under ultrasound guidance, 10 ml of 0.4% ropivacaine was injected around the superior trunk of the brachial plexus.
High dose group:Under ultrasound guidance, 15 ml of 0.4% ropivacaine was injected around the superior trunk of the brachial plexus.

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1.Patients who are unaware of their cancer diagnosis (as determined by Patients aged 18-74 years; 2.ASA ?~?; 3.BMI 18 ~ 30 kg/m2; 4. Elective Arthroscopic Rotator Cuff Repair Surgery.

Exclusion criteria

Exclusion criteria: 1.Refuse to perform nerve block; 2.Coagulation dysfunction; 3.Skin infection at the puncture site; 4.Allergy to local anesthetics; 5.Central system diseases, neuropathy of operative limbs, cervical disc herniation or cervical spondylosis; 6.History of severe cardiopulmonary function disease, such as chronic obstructive pulmonary disease or respiratory failure, existing phrenic nerve injury or paralysis on the contralateral side, and lobectomy on the contralateral side; 7.Long term chronic pain and related medication history; 8.The 24 hour follow up records were incomplete.

Design outcomes

Primary

MeasureTime frame
The incidence of hemidiaphragmatic paralysis at 30 minutes post nerve block ;

Secondary

MeasureTime frame
The degree of hemidiaphragmatic paralysis;The static and dynamic VAS scores at 0, 6, 12, and 24 hours postoperatively were compared among the three groups;Muscle strength and mobility of the affected (or surgical) upper limb were evaluated at 0, 6, 12, and 24 hours postoperatively in the three patient groups.;the duration of sensory block ;Medication status;Complications occurring ;Basic indicators: gender, age, BMI, ASA grade, comorbidities, history of previous surgery, special medication, type of surgery, operation time, extubation time, PACU residence time.;incidence of cardiovascular events;

Countries

China

Contacts

Public ContactLei Cao

Beijing Friendship Hospital, Capital Medical University

caoleijd@126.com+86 135 2054 6309

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 12, 2026