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Clinical study on continuous superior trunk block applied for the intra- and postoperative analgesic in arthroscopic shoulder surgery: a randomized controlled trial.

Clinical study on continuous superior trunk block applied for the intra- and postoperative analgesic in arthroscopic shoulder surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035957
Enrollment
Unknown
Registered
2020-08-20
Start date
2020-09-14
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

Intra- and postoperative pain in arthroscopic shoulder surgery

Interventions

STB group:continuous superior trunk block
IBPB group:continuous interscalene brachial plexus block

Sponsors

Sichuan Provincial Orthopedic Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Scheduled for elective unilateral arthroscopic shoulder surgery and the expected operation time is less than 2 hours; 2. Aged 18 to 70 years, regardless of gender; 3. American Society of Anesthesiologists (ASA) Physical Status classification I to II; 4. Body mass index was not less than 18.5 kg/?, and not more than 35 kg/?; 5. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. With a history of cardiac, renal, or hepatic disease; 2. Preexisting neurologic deficits or neuropathy affecting the brachial plexus; 3. Allergy to local anesthetics, or contraindications to peripheral nerve block; 4. Preexisting operative respiratory dysfunction.

Design outcomes

Primary

MeasureTime frame
Diaphragmatic Movement;VAS score;—

Secondary

MeasureTime frame
SPO2;related adverse reactions (dyspnea, hiccups, hoarseness, and Horner sign);Arterial blood gas analysis;Muscle strength;Sensory block;—

Countries

China

Contacts

Public ContactYin Wenchao

Sichuan Provincial Orthopedic Hospital

yinwenchao2018@163.com+86 15182720377

Outcome results

None listed

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