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Efficacy and Safety of the Distal Radial Approach (TunDRA)

Primary Purpose

Vascular Access Complication, Coronary Artery Disease

Status
Recruiting
Phase
Not Applicable
Locations
Tunisia
Study Type
Interventional
Intervention
distal radial artery approach
conventional radial artery approach
Sponsored by
General Administration of Military Health, Tunisia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vascular Access Complication focused on measuring Radial artery, coronary angiography, percutaneous coronary intervention, safety, efficacy, radial approach, anatomical snuff box

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Over 18 years old.
  • Hospitalized in the cardiology department of the military hospital of Tunis.
  • elective Percutaneous coronary intervention performed by experienced operators or fellows trained in the proximal and distal radial approach

Non-inclusion criteria:

  • not provided written informed consent
  • both radial arteries were used for prior catheterization
  • Under oral anticoagulation
  • Having coronary bypass surgery
  • Hemodynamic instability
  • contra-indication to the radial approach:

    • Orthopedic surgery: amputation
    • Severe burns of both upper limbs.
    • Radial artery pulse not palpable, negative modified Allen test or Barbeau classification type D
    • Identified radial vascular anomaly: stenosis, fistula, tortuosity not allowing passage of the catheter

Exclusion Criteria:

  • death within a short period of time after admission
  • PCI by the same puncture site will be performed within 30 days after the first puncture
  • lost to follow-up

Sites / Locations

  • Military hospital of TunisRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

distal radial artery approach

conventional radial artery approach

Arm Description

Elective percutaneous coronary intervention by forearm radial artery through the distal radial artery in the dorsum of the hand or the anatomical snuff-box

Elective percutaneous coronary intervention through conventional radial artery access

Outcomes

Primary Outcome Measures

Puncture success rate
Comparison of Puncture success rate between two groups: Distal Radial Access (DRA) and conventional Trans Radial Access (TRA)
Radial artery occlusion rate
Use of ALLEN and Barbeau tests, if abnormal, color Doppler ultrasound to assess the patency of the radial artery will be realized.

Secondary Outcome Measures

Crossover rate
Comparison of the access site crossover rate in each group to complete the staged procedure
Duration of the puncture
Exact measurement of puncture duration in seconds
Radial artery spasm
The incidence of vasospasm that necessitates additional medication or forces access site cross over is registered
Number of patients presenting hematoma
Hematoma according to Early Discharge After Transradial Stenting of Coronary Arteries Study (EASY) score, The score ranges from 1 (≤5 cm diameter) to 5 ( ischemic threat of the hand).
Pain scale
through 0-10 numeric pain rating scale, 0 being no pain and 10 being the worst pain imaginable
QuickDASH questionnaire
The Quick-Disabilities of the Arm, Shoulder and Hand (QuickDASH) score is used to assess hand function. The score ranges from 0 (no disability) to 100 (most severe disability)
Operator satisfaction
through 0-10 rating scale; 0 being very dissatisfied; 0 being very satisfied

Full Information

First Posted
March 17, 2022
Last Updated
April 4, 2022
Sponsor
General Administration of Military Health, Tunisia
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1. Study Identification

Unique Protocol Identification Number
NCT05311111
Brief Title
Efficacy and Safety of the Distal Radial Approach
Acronym
TunDRA
Official Title
Efficacy and Safety of the Distal Radial Approach in Percutaneous Coronary Interventions: Protocol of a Randomized Controlled Non-inferiority Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
May 30, 2022 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
General Administration of Military Health, Tunisia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this non-inferiority trial is to determine if the distal radial access (DRA) during percutaneous coronary intervention (PCI) has an acceptable efficacy compared to the reference access through the conventional radial artery (TRA) with a lower rate of radial artery occlusion (RAO) in real life practice.
Detailed Description
The conventional radial approach is the recommended vascular access for percutaneous coronary interventions. It is effective, feasible, but associated with a risk of occlusion of the radial artery. The distal radial approach is proposed as a new approach to reduce complications and preserve the radial artery. However, few clinical trials in real life were conducted in North African patients. This trial aims to evaluate the efficacy and safety of the distal radial approach versus the conventional radial approach. This trial is a non-inferiority, randomized controlled trial with two parallel arms: distal radial approach and conventional radial approach. Two hundred and fifty patients scheduled for percutaneous coronary intervention will be included. The two main endpoints are the puncture success rate with a non-inferiority margin of 10% and the rate of 30-day occlusion of the punctured radial artery. Secondary endpoints: catheterization success, crossover rate, procedure time, radial artery spasm, bleeding complications, QuickDASH score, pain score and operator satisfaction A single blind analysis will be led according to the per-protocol and intention-to-treat methods. Avoiding occlusion of the puncture site allows to preserve the radial artery for subsequent coronary or cerebral percutaneous interventions as well as for coronary bypasses and hemodialysis fistulas. The results will provide the parameters related to the efficacy and safety of the distal radial approach, so improving clinical practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Access Complication, Coronary Artery Disease
Keywords
Radial artery, coronary angiography, percutaneous coronary intervention, safety, efficacy, radial approach, anatomical snuff box

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, single-center, single-blind, randomized controlled trial
Masking
Outcomes Assessor
Masking Description
single blind during the analyze
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
distal radial artery approach
Arm Type
Experimental
Arm Description
Elective percutaneous coronary intervention by forearm radial artery through the distal radial artery in the dorsum of the hand or the anatomical snuff-box
Arm Title
conventional radial artery approach
Arm Type
Active Comparator
Arm Description
Elective percutaneous coronary intervention through conventional radial artery access
Intervention Type
Procedure
Intervention Name(s)
distal radial artery approach
Other Intervention Name(s)
DRA
Intervention Description
Procedure: Use of radial artery for access for a coronary angiography or intervention After preparation and local anesthesia, the operator will puncture the distal radial artery in the dorsum of the hand or the anatomical snuff-box. Then a sheath will be placed. A cocktail combining Risordan®, Loxen® and unfractionated heparin will be injected through the sheath. a wire will be introduced. At the end of the procedure, the sheath will be removed immediately and hemostasis by compression will be carried out with an elastic band for 12 hours. The choice of limb side, sheath, catheters will be chosen according to the operator's discretion.
Intervention Type
Procedure
Intervention Name(s)
conventional radial artery approach
Other Intervention Name(s)
TRA
Intervention Description
Procedure: conventional radial access for a percutaneous coronary intervention After preparation and local anesthesia, the operator will puncture the proximal radial artery at the conventional site in distal forearm. Then a sheath will be placed. A cocktail combining Risordan®, Loxen® and unfractionated heparin will be injected through the sheath. a wire will be introduced. At the end of the procedure, the sheath will be removed immediately and hemostasis by compression will be carried out with an elastic band for 12 hours. The choice of limb side, sheath, catheters will be chosen according to the operator's discretion.
Primary Outcome Measure Information:
Title
Puncture success rate
Description
Comparison of Puncture success rate between two groups: Distal Radial Access (DRA) and conventional Trans Radial Access (TRA)
Time Frame
During the procedure
Title
Radial artery occlusion rate
Description
Use of ALLEN and Barbeau tests, if abnormal, color Doppler ultrasound to assess the patency of the radial artery will be realized.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Crossover rate
Description
Comparison of the access site crossover rate in each group to complete the staged procedure
Time Frame
During the procedure
Title
Duration of the puncture
Description
Exact measurement of puncture duration in seconds
Time Frame
During the procedure
Title
Radial artery spasm
Description
The incidence of vasospasm that necessitates additional medication or forces access site cross over is registered
Time Frame
During the procedure
Title
Number of patients presenting hematoma
Description
Hematoma according to Early Discharge After Transradial Stenting of Coronary Arteries Study (EASY) score, The score ranges from 1 (≤5 cm diameter) to 5 ( ischemic threat of the hand).
Time Frame
24 hours
Title
Pain scale
Description
through 0-10 numeric pain rating scale, 0 being no pain and 10 being the worst pain imaginable
Time Frame
24 hours
Title
QuickDASH questionnaire
Description
The Quick-Disabilities of the Arm, Shoulder and Hand (QuickDASH) score is used to assess hand function. The score ranges from 0 (no disability) to 100 (most severe disability)
Time Frame
30 days
Title
Operator satisfaction
Description
through 0-10 rating scale; 0 being very dissatisfied; 0 being very satisfied
Time Frame
at the end of the inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Over 18 years old. Hospitalized in the cardiology department of the military hospital of Tunis. elective Percutaneous coronary intervention performed by experienced operators or fellows trained in the proximal and distal radial approach Non-inclusion criteria: not provided written informed consent both radial arteries were used for prior catheterization Under oral anticoagulation Having coronary bypass surgery Hemodynamic instability contra-indication to the radial approach: Orthopedic surgery: amputation Severe burns of both upper limbs. Radial artery pulse not palpable, negative modified Allen test or Barbeau classification type D Identified radial vascular anomaly: stenosis, fistula, tortuosity not allowing passage of the catheter Exclusion Criteria: death within a short period of time after admission PCI by the same puncture site will be performed within 30 days after the first puncture lost to follow-up
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aymen Noamen, MD
Phone
0021620215773
Email
no.aymen@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmed Ben Amara, fellow
Phone
0021654430166
Email
ahmedbenikhalled@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aymen Noamen, MD
Organizational Affiliation
military hospital of Tunis , Tunis EL manar University, Faculty of medicine of Tunis
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nadhem Hajlaoui, Pr
Organizational Affiliation
military hospital of Tunis , Tunis EL manar University, Faculty of medicine of Tunis
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Wafa Fehri, Pr
Organizational Affiliation
military hospital of Tunis , Tunis EL manar University, Faculty of medicine of Tunis
Official's Role
Study Chair
Facility Information:
Facility Name
Military hospital of Tunis
City
Tunis
ZIP/Postal Code
1008
Country
Tunisia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stambouli Nejla
Phone
0021655104234
Email
nejlastam@gmail.com
First Name & Middle Initial & Last Name & Degree
Aymen Noamen, MD
First Name & Middle Initial & Last Name & Degree
Ahmed Ben Amara, fellow

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36005910
Citation
Ben Amara A, Noamen A, Anouar Y, Chenik S, Hajlaoui N, Fehri W. Evaluation of the Distal Radial Approach in percutaneous coronary interventions. Controlled, randomized non-inferiority trial. Tunis Med. 2022 mars;100(3):192-202.
Results Reference
derived

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Efficacy and Safety of the Distal Radial Approach

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