Cleft Palate Clinical Trial
In cleft surgery there is no current general agreement on the treatment strategy of patients
with the Pierre Robin Sequence. The timing of surgery and the surgical approach depends on
the treating physician or the hospital facility. Literature regarding peri- and
postoperative complications in the target population are lacking.
The investigators aim to retrospectively review the charts of all cleft patients, both PRS
and non-PRS, treated with an adapted Furlow palatoplasty between 01/01/2011 and 31/08/2015.
The incidence of peri- and postoperative complications, with a specific focus on respiratory
complications, will be examined. The value of demographic, surgical and postoperative
parameters will be examined as potential risk factors for the development of complications.
n/a
Observational Model: Case Control, Time Perspective: Retrospective
Status | Clinical Trial | Phase | |
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Completed |
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Completed |
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N/A | |
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Completed |
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Withdrawn |
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Enrolling by invitation |
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Completed |
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Not yet recruiting |
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N/A | |
Completed |
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Completed |
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Completed |
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Phase 3 | |
Enrolling by invitation |
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Phase 4 | |
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Completed |
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Completed |
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N/A |