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Hemostatic Compression Patterns After Transradial Coronary Intervention (HCPATRI)

Primary Purpose

Coronary Disease

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
experimental group
control group
Sponsored by
First Affiliated Hospital Xi'an Jiaotong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Coronary Disease focused on measuring Coronary Disease, Radial artery occlusion, transradial coronary intervention

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients 18 years or older
  • Patients who received TRI for the first time

Exclusion Criteria:

  • Failure to puncture the radial artery in 1 attempt
  • Inaccessible radial arteries because of anatomic variations, such as hypoplastic radial arteries and radioulnar loop, which can be confirmed by radial artery angiography before the TRI
  • Patients who had previous radial procedure
  • Patients who were receiving IIb/IIIa receptor antagonist treatment

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Experimental

    Arm Label

    control group

    experimental group

    Arm Description

    Participants allocated to the control group will receive a routine long term postoperative puncture site compression via TR Band. In control group, TR Band deflation is commenced at the 2nd hour with successive 5 mL air released at 2 hours intervals until the bladder was empty at the 6th hour, and the TR Band is removed at the 24th hour.

    Participants allocated to the experimental group will receive a short term postoperative puncture site compression via TR Band. In experimental group, TR Band deflation is commenced at the 1st hour with 3 mL air released, and at the 2nd hour with 5ml, and at the 3rd hour with the remainder air in the bladder, and the TR Band is removed at the 12th hour.

    Outcomes

    Primary Outcome Measures

    RAO incidence
    At the 24th hour post TRI, RAO will be diagnosed via ultrasonic sound and RAO incidence will be evaluated between two groups.

    Secondary Outcome Measures

    postoperative puncture site bleeding incidence
    postoperative puncture site bleeding incidence will be studied in patient between two groups within 24 hours after TRI.
    patient comfort level
    At the 24th hour post TRI, patient comfort level will be evaluated by patients via a visual analogue scale for comfort level.

    Full Information

    First Posted
    September 4, 2016
    Last Updated
    September 20, 2016
    Sponsor
    First Affiliated Hospital Xi'an Jiaotong University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02895009
    Brief Title
    Hemostatic Compression Patterns After Transradial Coronary Intervention
    Acronym
    HCPATRI
    Official Title
    A Randomized Comparison of TR Band Hemostatic Compression Patterns After Transradial Coronary Intervention
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 2016 (undefined)
    Primary Completion Date
    January 2017 (Anticipated)
    Study Completion Date
    March 2017 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    First Affiliated Hospital Xi'an Jiaotong University

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of the study is to investigate the protective effects of short term TR Band compression on transradial coronary occlusion after transradial coronary intervention.
    Detailed Description
    Radial artery occlusion (RAO), an infrequent but serious complication after transradial coronary intervention (TRI), prevents subsequent use of the same radial artery for coronary angiography and intervention. Comparing to the overseas counterparts, most Chinese medical workers put more emphasis on prevention of postoperative puncture site bleeding, so longer compression hemostasis time is applied but this prolonged compression may underestimate or even ignore an increasing risk of RAO. Therefore, this study intends to compare short term TR Band compression and the routine long term one on transradial coronary occlusion after transradial coronary intervention. Participants allocated to the control group will receive a routine long term postoperative puncture site compression via TR Band. In control group, TR Band deflation is commenced at the 2nd hour with successive 5 mL air released at 2 hours intervals until the bladder was empty at the 6th hour, and the TR Band is removed at the 24th hour. Participants allocated to the experimental group will receive a short term postoperative puncture site compression via TR Band. In experimental group, TR Band deflation is commenced at the 1st hour with 3 mL air released, and at the 2nd hour with 5ml, and at the 3rd hour with the remainder air in the bladder, and the TR Band is removed at the 12th hour. At the 24th hour, RAO incidence, postoperative puncture site bleeding incidence and patient comfort level will be evaluated.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Coronary Disease
    Keywords
    Coronary Disease, Radial artery occlusion, transradial coronary intervention

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    control group
    Arm Type
    Other
    Arm Description
    Participants allocated to the control group will receive a routine long term postoperative puncture site compression via TR Band. In control group, TR Band deflation is commenced at the 2nd hour with successive 5 mL air released at 2 hours intervals until the bladder was empty at the 6th hour, and the TR Band is removed at the 24th hour.
    Arm Title
    experimental group
    Arm Type
    Experimental
    Arm Description
    Participants allocated to the experimental group will receive a short term postoperative puncture site compression via TR Band. In experimental group, TR Band deflation is commenced at the 1st hour with 3 mL air released, and at the 2nd hour with 5ml, and at the 3rd hour with the remainder air in the bladder, and the TR Band is removed at the 12th hour.
    Intervention Type
    Device
    Intervention Name(s)
    experimental group
    Intervention Description
    Participants allocated to the experimental group will receive a short term postoperative puncture site compression via TR Band. TR Band deflation is commenced at the 1st hour and completed at the 3rd hour, and the TR Band is removed at the 12th hour.
    Intervention Type
    Device
    Intervention Name(s)
    control group
    Intervention Description
    Participants allocated to the control group will receive a routine long term postoperative puncture site compression via TR Band. TR Band deflation is commenced at the 2nd hour and completed at the 6th hour, and the TR Band is removed at the 24th hour.
    Primary Outcome Measure Information:
    Title
    RAO incidence
    Description
    At the 24th hour post TRI, RAO will be diagnosed via ultrasonic sound and RAO incidence will be evaluated between two groups.
    Time Frame
    at the 24th hour post TRI
    Secondary Outcome Measure Information:
    Title
    postoperative puncture site bleeding incidence
    Description
    postoperative puncture site bleeding incidence will be studied in patient between two groups within 24 hours after TRI.
    Time Frame
    within 24 hours after TRI
    Title
    patient comfort level
    Description
    At the 24th hour post TRI, patient comfort level will be evaluated by patients via a visual analogue scale for comfort level.
    Time Frame
    at the 24th hour post TRI

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients 18 years or older Patients who received TRI for the first time Exclusion Criteria: Failure to puncture the radial artery in 1 attempt Inaccessible radial arteries because of anatomic variations, such as hypoplastic radial arteries and radioulnar loop, which can be confirmed by radial artery angiography before the TRI Patients who had previous radial procedure Patients who were receiving IIb/IIIa receptor antagonist treatment
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jingwen Hu, Master
    Phone
    008618991232872
    Email
    jingwenhu@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jingwen Hu, Master
    Organizational Affiliation
    First Affiliated Hospital Xi'an Jiaotong University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    2912567
    Citation
    Campeau L. Percutaneous radial artery approach for coronary angiography. Cathet Cardiovasc Diagn. 1989 Jan;16(1):3-7. doi: 10.1002/ccd.1810160103.
    Results Reference
    background
    PubMed Identifier
    8221875
    Citation
    Kiemeneij F, Laarman GJ. Percutaneous transradial artery approach for coronary stent implantation. Cathet Cardiovasc Diagn. 1993 Oct;30(2):173-8. doi: 10.1002/ccd.1810300220. Erratum In: Cathet Cardiovasc Diagn 1993 Dec;30(4):358.
    Results Reference
    background
    PubMed Identifier
    20506228
    Citation
    Rathore S, Stables RH, Pauriah M, Hakeem A, Mills JD, Palmer ND, Perry RA, Morris JL. A randomized comparison of TR band and radistop hemostatic compression devices after transradial coronary intervention. Catheter Cardiovasc Interv. 2010 Nov 1;76(5):660-7. doi: 10.1002/ccd.22615.
    Results Reference
    background
    PubMed Identifier
    24496325
    Citation
    Dai N, Xu DC, Hou L, Peng WH, Wei YD, Xu YW. A comparison of 2 devices for radial artery hemostasis after transradial coronary intervention. J Cardiovasc Nurs. 2015 May-Jun;30(3):192-6. doi: 10.1097/JCN.0000000000000115.
    Results Reference
    background
    PubMed Identifier
    26002786
    Citation
    Cong X, Huang Z, Wu J, Wang J, Wen F, Fang L, Fan M, Liang C. Randomized Comparison of 3 Hemostasis Techniques After Transradial Coronary Intervention. J Cardiovasc Nurs. 2016 Sep-Oct;31(5):445-51. doi: 10.1097/JCN.0000000000000268.
    Results Reference
    background
    PubMed Identifier
    22357780
    Citation
    Fech JC, Welsh R, Hegadoren K, Norris CM. Caring for the radial artery post-angiogram: a pilot study on a comparison of three methods of compression. Eur J Cardiovasc Nurs. 2012 Mar;11(1):44-50. doi: 10.1177/1474515111429656. Epub 2012 Jan 11.
    Results Reference
    background
    PubMed Identifier
    21584923
    Citation
    Pancholy SB, Patel TM. Effect of duration of hemostatic compression on radial artery occlusion after transradial access. Catheter Cardiovasc Interv. 2012 Jan 1;79(1):78-81. doi: 10.1002/ccd.22963. Epub 2011 May 16.
    Results Reference
    background

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    Hemostatic Compression Patterns After Transradial Coronary Intervention

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