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CompletedNCT02032069Updated Mar 15, 2016

Pneumoproteins Expression in the Organ Donor

An observational study in Primary Graft Dysfunction, sponsored by University Hospital of Mont-Godinne. Completed at 1 site in Belgium. Open to participants aged 5 Years to 70 Years. Per ClinicalTrials.gov, last updated 2016-03-15.

Sponsored by University Hospital of Mont-Godinne · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
20
Ages
5 Years to 70 Years
Sex
All
01

Study summary

Primary graft dysfunction, a form of reperfusion pulmonary edema that occurs early after lung transplantation, shares key clinical and pathological features with acute lung injury and its more severe form, the acute respiratory distress syndrome. However, in contrast to acute lung injury/acute respiratory distress syndrome, in which biomarkers in plasma, urine and lung edema fluid have prognostic and pathogenetic value, the role of biomarkers in primary graft dysfunction has been less thoroughly explored. We will try in this study de determine the rule of pneumoproteins in the donor organ on the pulmonary edema in the recipient.

02

Conditions studied

  • Primary Graft Dysfunction
03

In context

Primary Graft Dysfunction

26 studies on the registry are indexed under Primary Graft Dysfunction; 4 are open to participants now.

This study's enrollment of 20 is below the median of 60 across 13 observational studies indexed under Primary Graft Dysfunction.

Browse Primary Graft Dysfunction studies →

Lead sponsor

University Hospital of Mont-Godinne is the lead sponsor of 24 studies on the registry; 6 are open to participants now.

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

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Who can participate

Ages eligible
5 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Organ donors and lung recipients

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

All the organ donors for lung grafts.

Exclusion criteria

Exclusion Criteria:

none

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
20 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • NHBD

    Non Heart Beating Donors

    Other: no intervention

  • BDD

    Brain death donors

    Other: no intervention

Interventions

  • Otherno intervention
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What researchers measure

Primary outcomes

  1. Number of Recipient with primary graft dysfunction

    Time frame: one year

07

Study locations

1 site
  • CHU Mont-Godinne
    Yvoir, Namur 5530, Belgium
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2013, a primary completion of Jan 2016 and a completion of Jan 2016. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 6, 2014
First posted
Jan 9, 2014
Start
Jan 2013
Primary completionActual
Jan 2016
CompletionActual
Jan 2016
Last update
Mar 15, 2016
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02032069
Lead sponsor
University Hospital of Mont-Godinne
Responsible party
Asmae Belhaj (MD, University Hospital of Mont-Godinne) — Principal investigator
First posted
Jan 9, 2014
Start date
Jan 2013
Primary completion
Jan 2016
Completion
Jan 2016
Last update
Mar 15, 2016

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2016. You cannot join it, but the record below documents what was studied.

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Discussion

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