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Clinical Trials/NCT05892367
NCT05892367
Completed
Not Applicable

Transbrachial Access for Interventions in Patients With Peripheral Arterial Occlusive Disease: Evaluation of Local Complications With or Without Post-interventional Immobilization of the Upper Extremity

Wilhelminenspital Vienna1 site in 1 country95 target enrollmentJuly 10, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Complication of Treatment
Sponsor
Wilhelminenspital Vienna
Enrollment
95
Locations
1
Primary Endpoint
Occurrence of local complications at the puncture site
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of the present study is an evaluation, whether an immobilization of the upper extremity by means of a positioning splint can help to reduce the incidence of local complications after transbrachial puncture for peripheral arterial interventions, or not.

Detailed Description

Increasing numbers of peripheral arterial interventions are performed via transbrachial access leading to a higher number of local complications at the puncture site. Patients are demonstrating complications, such as hematoma, false aneurysm, secondary hemorrhage and arterial stenosis or occlusion. Due to not standardized post-interventional procedure regarding to immobilization a higher risk for local puncture site complication can occur. Usually, a compression bandage its applied to the brachial puncture site. Within this randomized study, patients randomized to the study group will receive an additional splint for 24 hours to ensure an immobilization of the affected arm. Following the removal of the compression dressing, and the splint in the study group, a duplex ultrasound its performed in order to detect local alterations and pathologies of the brachial artery. This examination is repeated for each patient in the course of an outpatient control six weeks post-interventionally. Pathologies are documented and treated if necessary.

Registry
clinicaltrials.gov
Start Date
July 10, 2018
End Date
October 2, 2020
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Wilhelminenspital Vienna
Responsible Party
Principal Investigator
Principal Investigator

Edda Skrinjar, M.D.

M.D.

Wilhelminenspital Vienna

Eligibility Criteria

Inclusion Criteria

  • Female and male patients suffering from peripheral arterial occlusive disease with indicated interventions via an transbrachial access (puncture of the left or right brachial artery)
  • age \> 18 years
  • approval to participate

Exclusion Criteria

  • unability or refusal to participate
  • dialysis patients/AV-fistula interventions
  • usage of closure devices

Outcomes

Primary Outcomes

Occurrence of local complications at the puncture site

Time Frame: 6 weeks

Local complications as hematoma, bleeding, pseudoaneurysm, arterial dissection, arterial stenosis, arterial occlusion, AV fistula detected by ultrasound 24 hours after intervention and at time of follow-up six weeks after treatment

Secondary Outcomes

  • Post-interventional pain at puncture site(24 hours)

Study Sites (1)

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