CClinicalTrials.gg
Status unknownNCT02299752Updated Nov 24, 2014

Unnoticed Gloves Perforation

An interventional study of single-gloving system and double-gloving system in Catheterization and Contamination, sponsored by International Institute of Rescue Research and Education. Status unknown at 1 site in Poland. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-11-24.

Sponsored by International Institute of Rescue Research and Education · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Nov 2014), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of the study was to investigate the incidence of glove perforation in cannulation of blood vessels (CBV) during resuscitation and compare perforation rates between single and double-gloves.

Read the detailed description

Exposure to blood pathogens among medical staff is a serious problem that should be first and foremost prevented . The risk of acquiring a virus from one percutaneous needle stick is 0.3% to 0.4% for human immunodeficiency virus (HIV), 6% to 30% for hepatitis B (HBV), and 2.7% to 10% for hepatitis C (HCV). The prevention of blood-borne infections is particularly important during cases when emergency medical attention is needed. Emergency Response Personnel that work in this profession have taken medical rescue courses to prepare for situations of sudden health threats, hence the majority of procedures is associated with direct contact with body fluids of the patient.

02

Conditions studied

  • Catheterization
  • Contamination
03

In context

Lead sponsor

International Institute of Rescue Research and Education is the lead sponsor of 36 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Give voluntary consent to participate in the study
  • Medical profession (paramedics, nurses, physicians) or medical students (nurses, paramedics, physicians)

Exclusion criteria

Exclusion Criteria:

  • Not meet the above criteria
  • Wrist or low back diseases
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Catheterization

    Blood vessel Catheterization during resuscitation with single and double - gloving system. Catheterization was performed using simulation mannikin

    Procedure: single-gloving system · Procedure: double-gloving system

Interventions

  • Proceduresingle-gloving system

    single-gloving system was used during Catheterization

  • Proceduredouble-gloving system

    double-gloving system was used during Catheterization. inner and outer gloves were the same size

06

What researchers measure

Primary outcomes

  1. visible puncture

    Checking gloves for visible damage in the course of cannulation during resuscitation

    Time frame: 1 day

Secondary outcomes

  1. WLT

    Water leak test was used to checking unnoticed gloves damage

    Time frame: 1 day

07

Study locations

1 of 1 sites recruiting
  • International Institute of Rescue Research and Education
    Warsaw, Masovia 03-122, Poland
    • Lukasz Czyżewski · Contact · rn.czyzewski@gmail.com · 725993850
    • Lukasz Szarpak · Principal investigator
    • Andrzej Kurowski · Sub investigator
    • Lukasz Czyżewski · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 24, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02299752
Lead sponsor
International Institute of Rescue Research and Education
Responsible party
Lukasz Szarpak (Lukasz Szarpak, National Institute of Cardiology, Warsaw, Poland) — Principal investigator
First posted
Nov 24, 2014
Start date
Nov 2014
Primary completion
Dec 2014 (estimated)
Completion
Dec 2014 (estimated)
Last update
Nov 24, 2014

Study contacts

Andrzej Kurowski
Contact
andrzejkurowski987@gmail.com
+48500186225
Lukasz Szarpak
principal investigator · Institute of Cardiology

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2014. You cannot join it, but the record below documents what was studied.

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