Effect of Furlow Palatoplasty With Buccal Myomucosal Flap on the Speech Development
ConditionCleft Palate
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age3-5
SponsorFayoum University
About this trial
About 20 patient will be collected according to the eligibility criteria and grouped into Group I : 10 patients were treated with furlow with buccinators flap Group II : 10 patients were treated with 2 flap palatoplasty All patients will be examined by an expert Phoniatrician by Recording of speech samples in Arabic language for the children in a soundproof room including repeated syllables, sentences with high-pressure sounds and counting from 1 to 10. The records will be analyzed to assess the degree of hypernasality, speech intelligibility and compensatory speech errors
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
3-5 years old childreen with previous treated complete cleft lip and palate, nonsyndromic.
lip and palate repair performed by one craniofacial surgeon
Disqualifiers
Patients with syndromic cleft lip.
Redu cases
Bilateral cleft lip
Patient older 5years or younger 3 years.
Trial population
3-5 year old children with treated cleft palate
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
furlow with buccal myomucosal flap
Procedure/Surgerypatients were treated with furlow with buccal myomucosal flap
two flap palatoplasty
Procedure/Surgerypatients were treated with two flap palatoplasty
Treatment groups
30 Participants
are divided into 2 treatment groupsGroup A: two flap palatoplasty group1 intervention
Group B: furlow with buccal myomucosal flap group1 intervention
Trial outcomes
Primary outcomes
1
nasopharyngoscopic examination
this will be done through the nasopharyngoscopic examination of the cleft patients after repair with Furlow with buccinator flap versus two flap palatoplasty. it will assess the grade of velopharyngeal closure during speech
Time frame
through study completion, an average one weekSponsors and contacts
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Source ClinicalTrials.gov