Lung Transplant Failure Clinical Trial
Official title:
Respiratory Physiotherapy as a Tool to Increase the Number of Solid Organ Donors
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.
Status | Recruiting |
Enrollment | 160 |
Est. completion date | April 2025 |
Est. primary completion date | April 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Organ donor older than 18yo Exclusion Criteria: - Absolute contraindications for MIE's use - Absolute contraindications for organ donation |
Country | Name | City | State |
---|---|---|---|
Spain | Irene bello | Barcelona |
Lead Sponsor | Collaborator |
---|---|
Vall d'Hebron Institute Research | Germans Trias i Pujol Hospital, Hospital Universitario Marqués de Valdecilla, Hospital Vall d'Hebron |
Spain,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The changes in Oxygenation | The changes of oxygenation comparing MIE to national protocol | Ten minutes after the MIE application and 60 minutes after MIE application or national protocol aplication | |
Secondary | Rate of complications with the use of MIE | To analyse the complications associated with the use of MIE in organ donors | During the intervention and 60 minutes after it. | |
Secondary | Number of potential lung donors | To analyse the increase in potential lung donors with MIE | during the recruitment time | |
Secondary | Number of lung donors | To analyse the increase in lung donors with MIE | during the recruitment time |
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