Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06522217
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-07-11
Brief Title:
Prosthetic Rehabilitation of Lip and Palate Deformaties in Neonates Using Two Different Approaches
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Prosthetic Rehabilitation of Lip and Palate Deformaties in Neonates Using Two Different Approaches
Status:
COMPLETED
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study was conducted to compare the use of conventional nasoalveolar molding appliances and the use of digitally designed and produced nasoalveolar molding appliances in rehabilitating neonates born with unilateral complete cleft lip and palate
Detailed Description:
For this prospective study twenty newborns with non-syndromic complete unilateral cleft lip and palate were referred from the Outpatient Clinics of several pediatric surgeons and obstetricians to the Department of Prosthodontics -Faculty of Dentistry - Tanta University
Inclusion criteria
Age range from 2-3 weeks after birth
Only the Non-syndromic unilateral cleft lip and palate neonates
Newborn infants without any surgical intervention
Exclusion criteria
Patients with the life threatening syndromes
Respiratory difficulties are not considered for presurgical treatment
Uncooperative guardians
Inclusion criteria
Age range from 2-3 weeks after birth
Only the Non-syndromic unilateral cleft lip and palate neonates
Newborn infants without any surgical intervention
Exclusion criteria
Patients with the life threatening syndromes
Respiratory difficulties are not considered for presurgical treatment
Uncooperative guardians
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None