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The Effect of Two Different Tourniquet Techniques on Peripheral IV Access Success Rates

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Mayo Clinic

Status

Completed

Conditions

Tourniquet

Treatments

Device: blood pressure cuff
Device: disposable elastic tourniquet

Study type

Interventional

Funder types

Other

Identifiers

NCT02389725
14-007501

Details and patient eligibility

About

The purpose of this study is to compare the success rates of two different tourniquets that are used when placing an IV.

Enrollment

121 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Emergency Department patients
  • 18 years old or older
  • who receive peripheral IV access

Exclusion criteria

  • Patients under the age of 18
  • prison inmates
  • pregnant patients
  • patients who are unable to give informed consent
  • critically ill patients who need emergent IV access as defined by the Emergency Medicine consultant of record for the patient

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

121 participants in 2 patient groups

disposable elastic tourniquet
Active Comparator group
Treatment:
Device: disposable elastic tourniquet
manual blood pressure cuff
Active Comparator group
Description:
manual blood pressure cuff inflated to 150 milliliters mercury (mmHg)
Treatment:
Device: blood pressure cuff

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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