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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06211205
Other study ID # NCT26091993123
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 30, 2024
Est. completion date June 30, 2025

Study information

Verified date January 2024
Source Cairo University
Contact Hana A Adawy
Phone +201002061202
Email hana_adel@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Lip taping was proven as simple, handy technique of PSIO for alveolar molding yielding enhanced maxillary arch dimensions in UCCLP infants. The approach behind this study is to combine this simple step with a digitally designed 3D printed customized nasal molding device to enhance the naslolabial esthetics and maxillary arch dimensions in infants with unilateral complete cleft lip and palate, employing full digital workflow.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date June 30, 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 30 Days
Eligibility Inclusion Criteria: 1. Infants with age range from 1-30 days. 2. Unilateral complete cleft lip and palate 3. Medically free subjects. 4. Both males and females. Exclusion Criteria: 1. Patients older than 30 days. 2. Syndromic patients with other defects in addition to cleft lip and palate. 3. Patients with bilateral cleft lip and palate. 4. Incomplete cleft lip. 5. Patient with previous surgical lip repair or adhesion. 6. Patients with previous presurgical infant orthopedic treatment. 7. Medically compromised patients.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Customized 3D printed nostril retainer combined with lip taping
the infants will receive a customised nostril retainer appliance to enhance the nasal esthetics combined with lip tape to approximate the labial and alveolar segments
Procedure:
Lip taping
the infants will receive lip tape to approximate the labial and alveolar segments

Locations

Country Name City State
Egypt Department of Orthodontics, Faculty of Dentistry, Cairo university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nasolabial esthetics Nasal basal width, Collumella Length, Defetcted Nostril width and height, Interlabial gap will be measured in mm at 2 time points to evaluate the effect of the intervention.
This will be performed on a 3D scan for the infants and through calibrated photographs
3 months
Secondary Maxillary arch changes Interalveolar gap will be measured in mm through an intraoral scan for the infants at 2 time points 3 months
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