MedTrace Logo

BIP ETT Clinical Tolerability, Safety and Performance Study

NCT01682486 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-06-20

No results posted yet for this study

Summary

The objective of the study is to determine Bactiguard coated BIP Endotracheal tube´s tolerability, safety and performance and compare it to a standard un-coated Endotracheal tube.

Conditions

  • Endotracheal Intubation During Surgery
  • Hospital Acquired Infections

Interventions

DEVICE

BIP ETT (Bactiguard)

Ventilation of surgery patients during anesthesia using BIP ETT

PROCEDURE

Standard ETT

Ventilation of surgery patients during anesthesia using standard ETT

Sponsors & Collaborators

  • Bactiguard AB

    lead INDUSTRY

Principal Investigators

  • Sigridur Kalman, MD PhD Prof · Karolinska University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • Sweden

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01682486 on ClinicalTrials.gov