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effects of the costoclavicular block in patients undergoing humeral fracture surgery

effects of the costoclavicular block in patients undergoing humeral fracture surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083782
Enrollment
Unknown
Registered
2024-05-01
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

proximal humeral fracture surgery

Interventions

costoclavicular group:None

Sponsors

Ningbo No.6 Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) American College of Anesthesiologists (ASA) grade ?~? 2) age: 18~75 years old 3) BMI :18~28kg/m2

Exclusion criteria

Exclusion criteria: 1) Patients refuse to participate in the study; 2) pre-existing neuropathy of the operative limb 3) pre-existing moderate-severe pulmonary disease (obstructive or restrictive) 4) coagulopathy 5) pregnancy 6) sepsis 7) hepatic failure (Child-Turcotte-Pugh score > 9) or renal failure (creatinine = 2 mg/dl or peritoneal dialysis or hemodialysis), 8) Allergy to amide local anesthetics; 9) chronic pain condition 10) prior surgery in the neck or infraclavicular region

Design outcomes

Primary

MeasureTime frame
pain scores before leaving PACU using a 0–10 numerical rating scale (0=no pain; 10=worst imaginable pain). ;

Secondary

MeasureTime frame
ipsilateral diaphragmatic excursion;FEV1;forced vital capacity, FVC;Sensory function scale;Motor function scale;

Countries

China

Contacts

Public Contactmiao zhu

Ningbo No.6 Hospital

zhumiao002@163.com+86 189 6984 2670

Outcome results

None listed

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