Timing of Primary Surgery for Cleft Palate

Information

  • Research Project
  • 7666755
  • ApplicationId
    7666755
  • Core Project Number
    U01DE018664
  • Full Project Number
    5U01DE018664-02
  • Serial Number
    18664
  • FOA Number
    PA-07-070
  • Sub Project Id
  • Project Start Date
    8/1/2008 - 16 years ago
  • Project End Date
    6/30/2013 - 11 years ago
  • Program Officer Name
    ATKINSON, JANE C
  • Budget Start Date
    7/1/2009 - 15 years ago
  • Budget End Date
    6/30/2010 - 14 years ago
  • Fiscal Year
    2009
  • Support Year
    2
  • Suffix
  • Award Notice Date
    5/19/2009 - 15 years ago

Timing of Primary Surgery for Cleft Palate

DESCRIPTION (provided by applicant): Isolated cleft palate is the commonest craniofacial birth anomaly (e.g., 4.5 per 10,000 births in the US). It creates problems in feeding, speech, hearing, and dental development. Unsuccessful surgery may fail to resolve these problems and reduce the child's potential for social development and inclusion. At this time there is an inadequate evidence base for selecting the optimal timing for surgery. There is however a plausible case for undertaking surgery at 6 months, rather than the more usual timing of 12 months, as the provision of a functioning palate when speech skills begin to develop may lead to better speech outcomes. A randomized control trial will be undertaken to compare the outcomes of surgery performed either at age 6 months or at age 12 months. All infants will receive the same type of palate surgery. Approximately 650 infants will be enrolled and followed until age 5 years. The key inclusion variables are that they have non-syndromic cleft palate, they have been independently judged to be medically fit for surgery, and their parents consent to participation. The main outcome will be insufficient velopharyngeal function assessed by blinded judges. Secondary outcomes will be surgical complications, articulation, hearing, and dentofacial development. Recruitment will take 3 years. The findings will be applicable to children with cleft palate in any part of the world. The clinical sites will be members of an international consortium of cleft centers who recently completed enrollment of 925 infants into large scale trials of unilateral cleft lip and palate sponsored by the European Commission and NIDCR: the Scandcleft Network (10 surgical sites serving all of Denmark, Finland, Norway and Sweden and five regional centers in the UK);and a large specialized cleft center in Brazil (USP-HRAC, Bauru). Project Narrative: Improving the evidence base for cleft palate surgery will improve the treatment and social integration of affected children, reduce the burden of remedial care that they and their families must endure, and reduce the cost of care associated with cleft palate.

IC Name
NATIONAL INSTITUTE OF DENTAL &CRANIOFACIAL RESEARCH
  • Activity
    U01
  • Administering IC
    DE
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    1076844
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    121
  • Ed Inst. Type
  • Funding ICs
    NIDCR:1076844\
  • Funding Mechanism
    Research Projects
  • Study Section
    ZDE1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    UNIVERSITY OF MANCHESTER
  • Organization Department
  • Organization DUNS
    229894910
  • Organization City
    MANCHESTER
  • Organization State
  • Organization Country
    UNITED KINGDOM
  • Organization Zip Code
  • Organization District
    UNITED KINGDOM