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Heparin for RAO Post-Transradial Angiography in AIS

Effectiveness and Safety of Heparinization for Radial Artery Occlusion After Transradial Cerebral Angiography in Patients With Acute Ischemic Stroke - A Multicenter, Prospective, Double-blind, Randomized Trail

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07162064
Enrollment
440
Registered
2025-09-09
Start date
2025-08-04
Completion date
2026-02-04
Last updated
2026-03-24

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

Conditions

Acute Ischemic Stroke

Brief summary

Cerebral angiography is a critical diagnostic tool in neurology, serving as the "gold standard" for evaluating cerebrovascular stenosis, hemodynamics, aneurysms, and arteriovenous malformations. Compared to the traditional transfemoral approach, transradial cerebral angiography (TRA) offers advantages such as preserved patient privacy, immediate post-procedure mobility, shorter hospitalization, and fewer access-site complications. Consequently, TRA has gained increasing acceptance among patients and clinicians as the preferred vascular access . However, radial artery occlusion (RAO) remains a common complication post-TRA, with reported incidence rates varying widely (1%-33%). RAO is particularly concerning as the radial artery serves as a key access for both cardiac and neurovascular interventions; its occlusion limits future procedural options.Evidence from interventional cardiology suggests that intra-arterial heparin administration significantly reduces RAO risk.However, patients undergoing transradial cerebral angiography are predominantly those with cerebrovascular diseases, including acute ischemic stroke (AIS)-a population at potential risk for hemorrhagic transformation.Although the 2022 Chinese Expert Consensus on Neurointerventional Diagnosis and Treatment via Transradial Access recommends intra-sheath heparin injection to prevent RAO, this recommendation is largely extrapolated from coronary intervention data. While several studies indicate that low-dose heparin is safe in moderate-to-severe AIS patients without increasing intracranial hemorrhage risk , high-level evidence specific to neurointerventional procedures-particularly in AIS patients-remains lacking.This multicenter, double-blind, randomized controlled trial (RCT) aims to: Evaluate the efficacy of intra-arterial heparin in preventing RAO following TRA cerebral angiography.Assess the safety of heparin in AIS patients, with a focus on hemorrhagic complications. By addressing these questions, the study will provide evidence-based guidance to optimize TRA outcomes, balancing RAO prevention with bleeding risk in neurovascular interventions. Its findings hold significant clinical value for improving the safety and efficacy of transradial cerebral angiography.

Interventions

Intra-arterial sheath injection of heparin 2500 units before operation

DRUGSaline (0.9% NaCl)

Intra-arterial sheath injection of 2mL saline (0.9% sodium chloride)

Sponsors

Xiang Luo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥18 years 2. Acute ischemic stroke onset within 7 days (inclusive) 3. Patients undergoing cerebral angiography via transradial approach 4. Participant or legal representative capable of providing informed consent

Exclusion criteria

1. Current anticoagulation therapy prior to procedure 2. Positive modified Allen's test result 3. History of coronary artery bypass grafting(CABG) with missing right radial artery graft 4. Severe forearm deformities (skin/musculoskeletal) or failed radial artery sheath placement 5. Suspected/confirmed pregnancy or lactation 6. Acute ischemic stroke with hemorrhagic transformation 7. Active systemic bleeding 8. Renal insufficiency (eGFR \<30 mL/min or serum creatinine \>200 μmol/L) 9. Investigator-determined ineligibility for trial participation

Design outcomes

Primary

MeasureTime frameDescription
24 hours radial artery occlusion rate after operation24 hours±12hoursRadial artery occlusion rate was assessed by ultrasonography 24 hours±12hours after the procedure.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026