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Superiorly Based Pharyngeal Flap Versus Myomucosal Resection and Direct Closure

Superiorly Based Pharyngeal Flap Versus Myomucosal Resection and Direct Closure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06343623
Enrollment
150
Registered
2024-04-02
Start date
2018-10-12
Completion date
2022-10-16
Last updated
2024-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Velopharyngeal Insufficiency

Brief summary

Patients were classified into two groups. Group (A) patients included fifty patients had velopharyngeal insufficiency and were surgically corrected by the superiorly based pharyngeal flap. Group (B) patients included fifty patients had velopharyngeal insufficiency and were surgically corrected with myomucosal resection and direct closure of the posterior pharyngeal wall

Detailed description

Patients were classified into two groups. Group (A) patients included fifty patients had velopharyngeal insufficiency and were surgically corrected by the superiorly based pharyngeal flap. Group (B) patients included fifty patients had velopharyngeal insufficiency and were surgically corrected with myomucosal resection and direct closure of the posterior pharyngeal wall

Interventions

PROCEDUREmyomucosal resection and direct closure

myomucosal resection and direct closure

PROCEDUREsuperiorly based flap

superiorly based pharyngeal flap

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* \- Patients have velopharyngeal insufficiency. * Age range 4-10 years

Exclusion criteria

* \- Syndromic patients.

Design outcomes

Primary

MeasureTime frameDescription
Improvement in the speech outcome4 yearsImprovement in the speech outcome using auditory perception assessment and videonasoendoscopy

Secondary

MeasureTime frameDescription
obstructive sleep apnea3 yearsobstructive sleep apnea using respiratory function test

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026