Fact CheckerSign in

NCT07162064CompletedPhase 3

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

Source: ClinicalTrials.gov · Last updated 24 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
440 (actual)
First submitted
26 Aug 2025
Start date
4 Aug 2025
Primary completion date
31 Jan 2026
Lead sponsor
Xiang Luo
Diseases
Stroke
NCT number
NCT07162064

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 440
  • From 4 Aug 2025 to the primary completion date, 31 Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current anticoagulation therapy prior to procedure

Other illness

  • History of coronary artery bypass grafting(CABG) with missing right radial artery graft
  • Acute ischemic stroke with hemorrhagic transformation
  • Active systemic bleeding

Lab values

  • Renal insufficiency (eGFR \<30 mL/min or serum creatinine \>200 μmol/L)

Other

  • Positive modified Allen's test result
  • Severe forearm deformities (skin/musculoskeletal) or failed radial artery sheath placement
  • Suspected/confirmed pregnancy or lactation
  • Investigator-determined ineligibility for trial participation

Who the study is looking for

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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tongji Hospital
Coordinator of this site? Confirm its status
WuhanChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.