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Feasibility and Outcomes of Repetitive Radial Approach

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ClinicalTrials.gov Identifier: NCT02017054
Recruitment Status : Withdrawn
First Posted : December 20, 2013
Last Update Posted : May 18, 2017
Sponsor:
Information provided by (Responsible Party):
Sheba Medical Center

Brief Summary:
The purpose of this study is to assess the feasibility of performing repetitive coronary angiograms via the radial approach

Condition or disease Intervention/treatment
Injury of Radial Artery Other: Cath

Detailed Description:
Assessing succes of radial access in patients with prior TRA procedures

Study Type : Observational [Patient Registry]
Actual Enrollment : 0 participants
Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration: 1 Month
Official Title: Feasibility and Outcomes of Repetitive Radial Approach
Study Start Date : January 2015
Estimated Primary Completion Date : December 2017
Estimated Study Completion Date : December 2017

Group/Cohort Intervention/treatment
Cath patients
Patients with previous cardiac cath via the radial access who are planned for additional radial access cardiac cath
Other: Cath
No intervention - registry
Other Name: No intervention - registry




Primary Outcome Measures :
  1. To assess patency of radial artery after repetitive radial artery access [ Time Frame: 1 month ]


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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with previous history of trans radial cardiac cath who are planned for additional trans radial cardiac cath
Criteria

Inclusion Criteria:

Patients with previous successful radial artery approach scheduled for elective transradial coronary angiography

Exclusion Criteria:

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


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02017054


Locations
Israel
Sheba Medical Center
Ramat Gan, Israel
Sponsors and Collaborators
Sheba Medical Center
Investigators
Principal Investigator: Amit Segev, MD Sheba MC

Responsible Party: Sheba Medical Center
ClinicalTrials.gov Identifier: NCT02017054     History of Changes
Other Study ID Numbers: SHEBA-13-0827-IB-CTIL
First Posted: December 20, 2013    Key Record Dates
Last Update Posted: May 18, 2017
Last Verified: May 2016