Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02398305
Other study ID # METc2011-233
Secondary ID
Status Completed
Phase N/A
First received December 4, 2014
Last updated March 24, 2015
Start date October 2012
Est. completion date August 2013

Study information

Verified date March 2015
Source University Medical Center Groningen
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

To obtain arterial access for a diagnostic cardiac catheterization or percutaneous coronary intervention (PCI) the cardiologist can choose between the femoral artery and the radial artery. In the University Medical Center Groningen the femoral artery is commonly used. After intervention the puncture site is closed with an arteriotomy closure device (ACD). Patients after radial access receive a pressure bandage at the puncture site, usually the Terumo (TR) wrist bandage.

The bedrest period for patients with an ACD is 1 hour after diagnostic cardiac catheterization and 2 hours after PCI. After the bedrest period patients are discharged 1 hour after diagnostic procedures or 4 hours after PCI. This to observe potential bleeding complications after the procedure. In patients with radial access, the TR bandage will be removed according to current protocol after 4 hours and additionally 1 hour observation is required. Several cardiologists have the intention to use the radial artery more frequent for cardiac catheterization or PCI. In a meta-analysis radial access is related to a 73% decrease in major bleeding complications compared to femoral access. Also there are no significant differences in MACE. Even so there are no differences in success percentage for cardiac catheterization or PCI and admission time is shorter for radial access (Am Heart J. 2009 Jan;157(1):132- 40). Admission time for diagnostic cardiac catheterization at the short-stay unit is in case of femoral access with an ACD approximately 2 hours. For patients after radial access post procedural admission time is approximately 5 hours. To guarantee patient throughput, uniformity of care and more efficient use of capacity of the short-stay unit, patients after radial access should not have a longer hospital admission time than patients after femoral access. Carrington et al. (J Interv Cardiol. 2009 Dec;22(6):571-5) have shown that it is safe to deflate the TR wrist band faster than four hours.

Objective of the study:

To describe the differences in safety, patient comfort and admission period after diagnostic cardiac catheterization through radial access, between the current protocol and the protocol of fast desufflation by Carrington et al.


Recruitment information / eligibility

Status Completed
Enrollment 173
Est. completion date August 2013
Est. primary completion date July 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnostic coronary angiogram

- Radial access

- 6 French sheath

Exclusion Criteria:

- Use of oral anticoagulants

- Percutaneous coronary intervention

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Device:
TR Band standard
Diminishing the air pressure in the TR Band following standard protocol
TR Band Quick
Diminishing the air pressure in the TR Band following a faster protocol

Locations

Country Name City State
Netherlands University Medical Centre Groningen Groningen

Sponsors (1)

Lead Sponsor Collaborator
University Medical Center Groningen

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bleeding Bleeding at puncture site after deflating pressure in TR band 1 year No
Secondary Swelling Swelling at puncture site that is not caused by bleeding 1 year No
Secondary Patient comfort Patient comfort, measured on VAS 1 year No
Secondary Time to discharge, after return on nursing unit 1 year No
See also
  Status Clinical Trial Phase
Completed NCT02343276 - Randomized Clinical Trial Comparing Transradial Catheterization With or Without Spasmolytic Drugs Phase 3