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Observation on the analgesic effects and safety of infraspinatus-teres minor interfascial block in patients undergoing arthroscopic shoulder surgery

Observation on the analgesic effects and safety of infraspinatus-teres minor interfascial block in patients undergoing arthroscopic shoulder surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105208
Enrollment
Unknown
Registered
2025-06-30
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Pain

Interventions

Group A:Ultrasound-guided interscalene block with injection of 20 ml of 0.33% ropivacaine
Group B:Ultrasound-guided combined suprascapular and axillary nerve block with injection of 10 ml of 0.33% ropivacaine to each nerve
GroupC:Ultrasound-guided infraspinatus-teres minor interfascial block with injection of 20 ml of 0.33% ropivacaine

Sponsors

Tianjin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients undergoing unilateral shoulder arthroscopy. 2.Age between 18 and 65 years (inclusive). 3.American Society of Anesthesiologists (ASA) physical status classification I to III. 4.The patient or the patient's legal representative is capable and willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with severe cardiac, hepatic, or renal disease, or coagulopathy. 2.Patients with pre-existing neurological deficits or pathologies affecting nerve block, or those who refuse regional anesthesia. 3.Patients with known allergy to local anesthetics, or infection, skin breakdown, or ulceration at the proposed puncture site(s). 4.Patients with psychiatric disorders precluding cooperation with the study procedures or follow-up. 5.Patients with opioid dependence. 6.Patients who decline patient-controlled analgesia (PCA). 7.Pregnant or lactating women. 8.Patients who refuse to participate in this study.

Design outcomes

Primary

MeasureTime frame
Postoperative VAS Scores;Rebound Tenderness Incidence;Diaphragm Thickness Change Rate and Diaphragm Excursion Pre- versus Postoperatively;Postoperative Quality of Recovery-15 (QoR-15) Score;

Secondary

MeasureTime frame
Intraoperative Anesthetic Consumption;Adverse Reaction Incidence;

Countries

China

Contacts

Public ContactLina Zhao

Department of Anesthesiology, Tianjin Hospital

zhalina1984@126.com+86 151 2204 6629

Outcome results

None listed

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