Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT05401669

Transradial Versus Transfemoral Access for Cerebral Angiography

Led by Huashan Hospital · Updated on 2024-09-04

748

Participants Needed

1

Research Sites

61 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is multi-center, prospective, randomized (1:1) controlled trial designed to assess and compare the feasibility, safety and success of Transradial access (TRA) versus Transfemoral access (TFA) for diagnostic cerebral angiography.

CONDITIONS

Official Title

Transradial Versus Transfemoral Access for Cerebral Angiography

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years old
  • Scheduled to undergo diagnostic cerebral angiography
  • Suitable for cerebral angiography via TRA and TFA access, with a radial artery diameter 2mm confirmed by ultrasonography
  • Modified Rankin Scale score 2
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Severe stenosis or significant vascular disease in radial, brachial, subclavian, brachiocephalic, iliac, or common femoral arteries that may block guidewire passage
  • Arteriovenous fistula for hemodialysis in the right upper limb
  • Planned interventional surgery within 24 hours after initial angiography
  • Need for cerebral angiography in an emergency department
  • Use of general anesthesia
  • Contraindications to cerebral angiography such as allergy or intolerance to contrast media, severe coagulation disorders, arterial dissection, puncture site infection, or renal insufficiency (Creatinine > 3 times upper limit of normal)
  • Women who are pregnant or planning to become pregnant within 1 year
  • Participation in another clinical trial
  • Any other condition considered unsuitable by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Huashan Hospital

Shanghai, Shangai, China, 200000

Actively Recruiting

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Research Team

H

Heng Yang, PhD, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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