Etiological Study of Persistent Velopharyngeal Insufficiency in Children With Operated Velopalatine Cleft by Analysis of Velopharyngeal Motor Skills in Static and Dynamic MRI
FENTIRM
1 other identifier
interventional
30
1 country
1
Brief Summary
Velopharyngeal insufficiency is defined as the inability of the soft palate to isolate the nasopharynx from the oropharynx. It is a frequent sequela in patients with a velopalatine cleft despite anatomical restoration of the soft palate by intravelar veloplasty at 6 months. If rehabilitation by a speech therapist is not successful, a pharyngoplasty can be discussed. In the last ten years, MRI was used in dynamic and static way, to analyzed velopharyngeal muscles, in particular Levator Veli Palatini. MRI could be used to identify the etiology of VPI in those patients, and thus allow personalized rehabilitation and surgical management. The aim of this study is to examine the differences in velopharyngeal motricity as well as velar muscles morphology, positioning, and symmetry of children with repaired cleft palate with different degrees of severity of velopharyngeal insufficiency (VPI), and children with labial cleft (noncleft palate anatomy).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2023
CompletedFirst Submitted
Initial submission to the registry
October 3, 2023
CompletedFirst Posted
Study publicly available on registry
October 10, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2024
CompletedOctober 10, 2023
October 1, 2023
1 year
October 3, 2023
October 3, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
ratio between the diameter of pharynx at rest and during phonation.
day 1
closure distance between the velar knee and the posterior pharyngeal wall
day 1
distance between the velar knee and the posterior pharyngeal wall
day 1
Study Arms (4)
child with operated isolated labial cleft
EXPERIMENTALchild with isolated operated velopalatal cleft with severe VPI ( IIB//IIM) and normal velum anatomy
EXPERIMENTALchild with isolated operated velopalatal cleft with soft VPI (I/I-II) and abnormal velum anatomy
EXPERIMENTALchild with isolated operated velopalatal cleft with normal anatomy and soft VPI
EXPERIMENTALInterventions
ubjects will be scanned in the supine position using ACHIEVA 3T TX DStream Philips® and a 33 channels head and neck coil. An elastic strap will be fixed to the forehead to limits movement during scan. Headset will be used to cancel the loud MRI noise and to communicate with the subjects
Eligibility Criteria
You may qualify if:
- Children aged 7 to 12 years with Isolated cleft lip
- isolated velopalatal cleft
- Without a diagnosis of syndromic cleft or Pierre Robin sequence
- French speaking, and French is the native language
- Operated with a cheiloplasty (for cleft lip) or an intravelar Veloplasty (according to Sommerlad) at the Amiens University Hospital
- Whose follow-up is done at the Amiens University Hospital
You may not qualify if:
- Refusal of the parents and/or the patient
- With a contraindication to MRI
- Whose follow-up was initiated in another center and/or whose surgery was performed in another center
- Whose surgical schedule has not been followed
- Patient with severe neurological or neuropsychiatric disorders or Severe speech and language delay not related to the cleft anatomy
- Patients treated with fixed, non-removable orthodontic treatment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Amiens-Picardie
Amiens, 80054, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 3, 2023
First Posted
October 10, 2023
Study Start
October 1, 2023
Primary Completion
October 1, 2024
Study Completion
December 1, 2024
Last Updated
October 10, 2023
Record last verified: 2023-10
Data Sharing
- IPD Sharing
- Will not share