FIXATUB: "Comparison of Two Methods of Securing Endotracheal Tubes in Intensive Care : Elastic Adhesive Strips vs Lace In A Protective Sheath."

Sponsor
Centre Hospitalier Departemental Vendee (Other)
Overall Status
Recruiting
CT.gov ID
NCT04819425
Collaborator
(none)
768
15
2
19.2
51.2
2.7

Study Details

Study Description

Brief Summary

Every year, in France, nearly 100,000 patients hospitalized in intensive care more than 48 hours require invasive respiratory assistance via an endotracheal tube.

Appropriate tube fixation is essential to ensure effective ventilation while minimizing potential complications such as accidental extubations. However, the fixation system chosen may lead to peribuccal lesions such as bedsores, shearing or cutaneous-mucous tear. These lesions are painful for patients and often unsightly as scar may remain.

There are no formal recommendations for the use of any type of fixing system. Thus, systems used to secure the endotracheal tube vary from one ICU to another.

The objective of this study is to demonstrate that the fixing strategy by elastic adhesive tape reduces the risk of developing a peribuccal lesion during the time of the endotracheal tube's maintenance.

Condition or Disease Intervention/Treatment Phase
  • Device: Elastic Adhesive Strips
  • Device: Lace in A Protective Sheath
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
768 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Cluster and CrossoverCluster and Crossover
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
"Comparison of Two Methods of Securing Endotracheal Tubes in Intensive Care : Elastic Adhesive Strips vs Lace In A Protective Sheath. A Randomized Multicenter, Cluster and Crossover Controlled Study. FIXATUB"
Actual Study Start Date :
Jun 28, 2021
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Feb 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Elastic Adhesive Strips

Endotracheal tube fixed by elastic adhesive tape (Tensoplast type adhesive tape): The adhesive tape will be attached to the patient's face (opposite side to the endotracheal tube) and then two turns around the endotracheal tube will be made. The rest of the adhesive tape will be attached to the other side of the face (side of the endotracheal tube). The laminated tape will be kept on the adhesive tape until it passes over the neck in order to avoid adhering to the hair. Finally, the end of the adhesive tape will be replaced on the part already attached to the patient. It will be changed daily and after stain or examinations if necessary.

Device: Elastic Adhesive Strips
Securement of Endotracheal tube with Elastic Adhesive Strips

Active Comparator: Lace in A Protective Sheath

A loop is made with the lace then the endotracheal tube is passed through the loop. The loop is tightened by pulling each side on the remaining cords and a knot is made on one side of the fastener. It will be changed daily and after stain or examinations if necessary.

Device: Lace in A Protective Sheath
Securement of Endotracheal tube with Lace in A Protective Sheath

Outcome Measures

Primary Outcome Measures

  1. Peribuccal lesion [up to 10 days after intubation]

    Appearance of at least one peribuccal lesion during the first 10 days of maintaining the endotracheal tube inserted orally. Presence of peribuccal lesion will be validated on picture by an independent review committee. The picture will be taken daily without the visible fixing system (blind maintained for the adjudication committee) from J0 to J10 at the site of the endotracheal tube.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient hospitalized in Intensive Care Unit

  • Age over 18

  • Intubation for estimated duration > 48h

  • Patient treated with vasopressors

  • Patient or relative who received the information and are not opposed to study participation.

Exclusion Criteria:
  • Pre-existing face lesions at ICU admission along the path of the endotracheal tube fixing.

  • Admitted patient already intubated upon transfer from another ICU

  • Nasotracheal intubation

  • Admitted tracheotomized patient

  • Patient under guardianship/curatorship,

  • Pregnant, nursing, parturient woman

  • Lack of social security affiliation

  • Moribund

  • Incapable major (under guardianship, curatorship)

  • Patient deprived of liberty by judicial decision

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier d'Angoulême Angoulême France
2 CH Victor Dupouy Argenteuil France
3 Centre Hopitalier La Rochelle La Rochelle France
4 Centre Hospitalier Le Mans Le Mans France
5 Groupe Hospitalier Bretagne Sud Lorient France
6 CHU Nantes Hôtel Dieu Nantes France
7 CHU Nantes Hôtel Dieu Nantes France
8 Centre Hospitalier Régional d'Orléans Orléans France
9 CHI Poissy - Saint-Germain-en-Laye Poissy France
10 CHU de Poitiers Poitiers France
11 Hôpital Nord Laennec Saint-Herblain France
12 CH Saint-Nazaire Saint-Nazaire France
13 CHU La Réunion GHSR Saint-Pierre France
14 CHU La Réunion GHSR Saint-Pierre France
15 CHU de Tours Tours France

Sponsors and Collaborators

  • Centre Hospitalier Departemental Vendee

Investigators

  • Principal Investigator: Vanessa ZINZONI, CHD Vendée

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Departemental Vendee
ClinicalTrials.gov Identifier:
NCT04819425
Other Study ID Numbers:
  • CHD032-20
First Posted:
Mar 29, 2021
Last Update Posted:
Mar 28, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre Hospitalier Departemental Vendee

Study Results

No Results Posted as of Mar 28, 2022