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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02017028
Other study ID # SHEBA-13-0824-IB-CTIL
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 2015
Est. completion date December 30, 2016

Study information

Verified date May 2016
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of this study is to investigate the relation between the previous presence of endothelial dysfunction and the development of radial artery vasospasm during the trans-radial coronary evaluation.


Description:

All patient will undergo pre procedural endoPAT assessment for endothelial dysfunction


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 30, 2016
Est. primary completion date December 30, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: Patients without angiographic proof of coronary disease, with scheduled elective coronary angiographic evaluation by radial approach. Exclusion Criteria: Impossibility to perform radial approach; abnormal Barbeau test result (type C and D); previous important trauma of the upper limbs; presence of fistule for renal dialysis; lymphedema; acute myocardial infarction, severe valvular heart disease; patients with NYHA class III and IV heart failure; malignancy; active myocarditis; HIV infection or immunodeficiency state; chronic viral infection; acute systemic infection requiring antibiotics; systemic inflammatory disease; Raynaud's syndrome; refusal to sign the informed consent form. All participants must give a written informed consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba Medical center Ramat Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary To assess relation between the presence of previous endothelial dysfunction and radial artery vasospasm 1 month
See also
  Status Clinical Trial Phase
Terminated NCT04457219 - Assessment of Radial Artery Complications Whilst Achieving Rapid Haemostasis N/A