Respiratory Physiotherapy as a Tool to Increase the Number of Solid Organ Donors

NCT ID: NCT06202859

Last Updated: 2024-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-11-01

Study Completion Date

2025-04-30

Brief Summary

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The main objective of the project is to determine the variation of PaO2 / FiO2 (PaFi) after the use of mechanical insufflation-exsufflation (MI-E) or mechanical cough assistant in the donor in brain death (DBD) and in the potential donor in control donor after circulatory death (cDCD) It is a randomized prospective multicentre study. Four centres with a solid organ donation program will participate in the study, the Hospital Clínic i Provincial de Barcelona (HCB), the Germans Tries y Pujol Hospital (HGTP), the Marqués de Valdecilla Hospital (HMV) and the Vall d'Hebron Hospital (HVH). One hundred and sixty consecutive eligible donors will be included in DBD and cDCD older than 18 years.

* P1: Eighty donors will be maintained following national guidelines.
* P2: Eighty donors will be maintained following national guidelines and:
* Manual techniques of secretion drainage
* Two sequences separated for 1 min of 6 cycles each of MI-E(Cough Assist E70, Respironics Philips.

Demographic variables of the donor and recipient will be collected, as well as differences in PaFi, static compliance, and radiographic changes between P1 and P2 donors. The percentage of lung donors recovered by P2 with respect to P1 will be analyzed.

Detailed Description

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Conditions

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Lung Transplant Failure

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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MIE group

* Manual techniques of secretion drainage
* Two sequences separated for 1 min of 6 cycles each of MI-E(Cough Assist E70, Respironics Philips.

Group Type EXPERIMENTAL

MIE

Intervention Type DEVICE

Two sequences separated for 1 min of 6 cycles each of MI-E(Cough Assist E70, Respironics Philips.

Control group

Maintained following national guidelines.

Group Type ACTIVE_COMPARATOR

MIE

Intervention Type DEVICE

Two sequences separated for 1 min of 6 cycles each of MI-E(Cough Assist E70, Respironics Philips.

Interventions

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MIE

Two sequences separated for 1 min of 6 cycles each of MI-E(Cough Assist E70, Respironics Philips.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Organ donor older than 18yo

Exclusion Criteria

* Absolute contraindications for MIE's use
* Absolute contraindications for organ donation
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospital Vall d'Hebron

OTHER

Sponsor Role collaborator

Germans Trias i Pujol Hospital

OTHER

Sponsor Role collaborator

Hospital Universitario Marqués de Valdecilla

OTHER

Sponsor Role collaborator

Vall d'Hebron Institute Research

OTHER

Sponsor Role lead

Responsible Party

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Irene Bello

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Irene bello, Professor

Role: STUDY_CHAIR

Vall d'Hebron Institute of Research

Locations

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Irene bello

Barcelona, , Spain

Site Status RECRUITING

Countries

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Spain

Central Contacts

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Irene bello, Professor

Role: CONTACT

620664172

Facility Contacts

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Irene bello, Prof

Role: primary

620664172

References

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Reference Type BACKGROUND
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Reference Type BACKGROUND
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Reference Type BACKGROUND
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Reference Type BACKGROUND
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Other Identifiers

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MIE-don study

Identifier Type: -

Identifier Source: org_study_id

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