An Investigation for the Optimal Timing of a Cleft Palate Repair
Primary Purpose
Cleft Palate
Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Palatoplasty
Palatoplasty
Sponsored by
About this trial
This is an interventional treatment trial for Cleft Palate focused on measuring pediatric, cleft palate, plastic surgery, palatoplasty, pharyngoplasty
Eligibility Criteria
Inclusion Criteria:
- Infant diagnosed with non-syndromic isolated unrepaired cleft involving the secondary palate.
- Between newborn and 5 months of age (pre-palate surgical assessment/ consultation.
- Treated at SickKids.
Exclusion Criteria:
- If they are non-Ontario residents;
- If they have clinical features suggestive of an associated syndrome and/or an associated syndrome;
- If they have Pierre Robin sequence;
- If the palate repair cannot be performed before 15 months of age;
- If the extent of clefting is limited to the primary palate or submucous cleft of the soft palate;
- If the child have a combined cleft lip and palate diagnosis
Sites / Locations
- The Hospital for Sick Children
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Group A
Group B
Arm Description
Early Cleft Palate Repair (Age group 6-10 months)
Sick Kids Routine cleft palate repair (age group 10-14 months)
Outcomes
Primary Outcome Measures
The primary outcome will be determined by the presence/absence of Velopharyngeal Insufficiency (VPI) at 5 years of age.
Secondary Outcome Measures
Surgical Complications: Surgical complications (i.e. fistula and dehiscence) will be evaluated between 6-8 weeks post-operatively and recorded.
Feeding Assessment: A feeding assessment will be conducted pre-surgery (5 months of age) and post surgery (6-8 weeks post-operatively).
Dental and Facial Growth Disturbances measured in patients with isolated secondary plate cleft by analysis of the severity of their malocclusion,and performing a lateral cephalometric analysis
Full Information
NCT ID
NCT00779961
First Posted
October 23, 2008
Last Updated
March 23, 2022
Sponsor
The Hospital for Sick Children
1. Study Identification
Unique Protocol Identification Number
NCT00779961
Brief Title
An Investigation for the Optimal Timing of a Cleft Palate Repair
Official Title
An Investigation for the Optimal Timing of a Cleft Palate Repair
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 2008 (undefined)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hospital for Sick Children
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The effect of timing of cleft palate repair on speech development, velopharyngeal functioning, and facial growth remains unknown. The objective of this study is to determine the effectiveness of early palatal repair versus The Hospital for Sick Children (SickKids) routine palatal repair in isolated cleft palate patients by comparing speech development, velopharyngeal functioning and facial growth outcomes. The null hypothesis is no difference in speech development, velopharyngeal functioning and facial growth between early palatal repair and SickKids routine palatal repair in isolated cleft palate patients.
Detailed Description
The goals of palatoplasty are to provide an intact palate and to create a normally functioning velopharyngeal mechanism as early as possible without hazard to other aspects of health and development. Two major criteria by which the success of cleft palate surgery is determined are subsequent speech development and facial growth. Therefore, the debate about timing of cleft palate surgery is focused on the need for early palatoplasty for speech purposes versus later palatoplasty to ensure undisturbed facial growth. A compromise solution to this controversy was proposed by Schweckendiek; the soft palate is repaired at an early age leaving the hard palate cleft unrepaired until later in life. The premise is that primary veloplasty will result in a functioning velopharyngeal mechanism for early speech development, while the unrepaired hard palate will allow unrestricted maxillary growth. The speech outcomes of patients who have undergone delayed stage palate repair have been addressed in several studies and case series. However, there is little evidence to support the benefits of delayed stage repair with respect to facial growth and speech development. Results from published studies have shown the speech results to be relatively poor and fistula rates as unacceptably high. These results have lead a vast majority of North American surgeons to favour primary one-stage repair. Yet, the optimum timing of primary palate repair remains unknown. No randomized control trials or prospective cohort studies have been conducted to address this question.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cleft Palate
Keywords
pediatric, cleft palate, plastic surgery, palatoplasty, pharyngoplasty
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
320 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group A
Arm Type
Experimental
Arm Description
Early Cleft Palate Repair (Age group 6-10 months)
Arm Title
Group B
Arm Type
Active Comparator
Arm Description
Sick Kids Routine cleft palate repair (age group 10-14 months)
Intervention Type
Procedure
Intervention Name(s)
Palatoplasty
Intervention Description
Routine palatoplasty will be performed under the supervision of one of five surgeons within the Division of Plastic Surgery at Sick Kids
Intervention Type
Procedure
Intervention Name(s)
Palatoplasty
Intervention Description
Palatoplasty will be performed under the supervision of one of five surgeons within the Division of Plastic Surgery at Sick Kids
Primary Outcome Measure Information:
Title
The primary outcome will be determined by the presence/absence of Velopharyngeal Insufficiency (VPI) at 5 years of age.
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Surgical Complications: Surgical complications (i.e. fistula and dehiscence) will be evaluated between 6-8 weeks post-operatively and recorded.
Time Frame
6-8 weeks post-op
Title
Feeding Assessment: A feeding assessment will be conducted pre-surgery (5 months of age) and post surgery (6-8 weeks post-operatively).
Time Frame
6-8 weeks post-op
Title
Dental and Facial Growth Disturbances measured in patients with isolated secondary plate cleft by analysis of the severity of their malocclusion,and performing a lateral cephalometric analysis
Time Frame
5 years of age, 11-13 years of age
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
5 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Infant diagnosed with non-syndromic isolated unrepaired cleft involving the secondary palate.
Between newborn and 5 months of age (pre-palate surgical assessment/ consultation.
Treated at SickKids.
Exclusion Criteria:
If they are non-Ontario residents;
If they have clinical features suggestive of an associated syndrome and/or an associated syndrome;
If they have Pierre Robin sequence;
If the palate repair cannot be performed before 15 months of age;
If the extent of clefting is limited to the primary palate or submucous cleft of the soft palate;
If the child have a combined cleft lip and palate diagnosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David M Fisher, MD, FRCSC
Organizational Affiliation
The Hospital for Sick Children, Toronto, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
An Investigation for the Optimal Timing of a Cleft Palate Repair
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