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NCT02389725 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by Mayo Clinic.

Completed
Registry status
NA
Development phase
121
Enrollment target

NCT02389725: Completed NA study, sponsored by Mayo Clinic.

NCT02389725 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 121 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02389725, a NA study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
NA
Development phase
121 participants
Enrollment target

Study Summary

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

Primary Outcome

Peripheral IV access success rate is defined as the number of subjects who had successful peripheral intravenous cannulation on the first attempt. An attempt was defined as a needle penetrating the surface of the subject's skin. Successful access was defined as good flow through an IV catheter with a saline flush and without subcutaneous fluid collection.

Interventions

  • DEVICE blood pressure cuff
  • DEVICE disposable elastic tourniquet

Trial Details

FieldValue
Enrollment Target 121 participants
Start Date 2015-04
Est. Completion 2016-06
Phase NA
Mayo Clinic

2,844 total trials

What the finished NCT02389725 record still lists

NCT02389725 is an interventional study that assigns participants to a tested intervention. The registered 121 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 2 interventions - of which blood pressure cuff is the first listed.

NCT02389725 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02389725 about?

NCT02389725 is a clinical study titled "The Effect of Two Different Tourniquet Techniques on Peripheral IV Access Success Rates". The purpose of this study is to compare the success rates of two different tourniquets that are used when placing an IV.

What is the current status of trial NCT02389725?

This trial is currently completed. It is a NA study. The enrollment target is 121 participants. The study started on 2015-04. Estimated completion is 2016-06.

What interventions are being tested in trial NCT02389725?

The interventions under investigation include: blood pressure cuff (DEVICE), disposable elastic tourniquet (DEVICE).

Who is sponsoring clinical trial NCT02389725?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02389725's enrollment target sits among peer trials

121 762nd of 2000 higher than 1,239 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02389725, the US trial registry maintained by the National Library of Medicine. NCT02389725 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.