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Effects of Radial Nerve Block at the Elbow Combined with Musculocutaneous Nerve Block on the Safety and Long-term Complications of Coronary Angiography

Effects of Radial Nerve Block at the Elbow Combined with Musculocutaneous Nerve Block on the Safety and Long-term Complications of Coronary Angiography

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123405
Enrollment
Unknown
Registered
2026-04-26
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Coronary heart disease

Interventions

Radial nerve block combined with musculocutaneous nerve block group:Ultrasound-guided combined radial nerve and musculocutaneous nerve block at the elbow
Local Infiltration Group:Simple Local Infiltration Group

Sponsors

Department of Anesthesiology, the 940th Hospital of Joint Logistics Support Force of People Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 18-90 years, ASA classification I-I; 2. Indication for coronary angiography; 3. Good radial artery pulse, and meets any of the following: (1) Negative modified Allen test (palm color returns within 10 seconds); (2) Ultrasound confirms the radial-ulnar palmar arch is unobstructed; 4. Voluntarily participates and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Diseases that increase the risk of bleeding or thrombosis; 2. Severe cardiac dysfunction (NYHA class IV); 3. Allergic history: allergy to the drugs used (local anesthetics, contrast agents, dexamethasone, heparin, P2Y12 receptor antagonists), or severe uncontrolled hypertension; 4. Issues at the puncture site: infection, skin disease, arteriovenous atrophy, or local nerve function abnormalities at the intended puncture site; 5. Severe liver or kidney dysfunction; 6. Cognitive impairment or mental illness preventing cooperation; 7. Pregnant or breastfeeding women; 8. Other conditions deemed by the investigator to make participation inappropriate (e.g., expected survival <1 year).

Design outcomes

Primary

MeasureTime frame
NRS pain scores at different time points;

Secondary

MeasureTime frame
Radial artery spasm;radial artery diameter;

Countries

China

Contacts

Public ContactZhang Xueying

Department of Anesthesiology, the 940th Hospital of Joint Logistics Support Force of People Liberation Army

1723300253@qq.com+86 190 3960 9314

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026