Feasibility and Outcomes of Repetitive Radial Approach
1 other identifier
observational
N/A
1 country
1
Brief Summary
The purpose of this study is to assess the feasibility of performing repetitive coronary angiograms via the radial approach
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Jan 2015
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 10, 2013
CompletedFirst Posted
Study publicly available on registry
December 20, 2013
CompletedStudy Start
First participant enrolled
January 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2017
CompletedMay 18, 2017
May 1, 2016
2.9 years
December 10, 2013
May 17, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
To assess patency of radial artery after repetitive radial artery access
1 month
Study Arms (1)
Cath patients
Patients with previous cardiac cath via the radial access who are planned for additional radial access cardiac cath
Interventions
Eligibility Criteria
Patients with previous history of trans radial cardiac cath who are planned for additional trans radial cardiac cath
You may qualify if:
- Patients with previous successful radial artery approach scheduled for elective transradial coronary angiography
You may not qualify if:
- Lack of indication to perform radial approach Abnormal Barbeau test result (type C and D) Presence of radial artery occlusion Previous important trauma of the upper limbs Presence of fistula for renal dialysis Lymphoedema Acute myocardial infarction Refusal to sign the informed consent form
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sheba Medical Center
Ramat Gan, Israel
Study Officials
- PRINCIPAL INVESTIGATOR
Amit Segev, MD
Sheba MC
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Month
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 10, 2013
First Posted
December 20, 2013
Study Start
January 1, 2015
Primary Completion
December 1, 2017
Study Completion
December 1, 2017
Last Updated
May 18, 2017
Record last verified: 2016-05