Effect of Novel Nasoalveolar Molding Techniques on Parents' Satisfaction and Short Term Treatment Outcomes in Unilateral Cleft Lip and Palate Infants: A Randomized Controlled Trial
Primary Purpose
Cleft Lip and Palate
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Modified Nasoalveolar molding
Taping
CAD/NAM
Sponsored by
About this trial
This is an interventional treatment trial for Cleft Lip and Palate
Eligibility Criteria
Inclusion Criteria:
- Infants with age range from 7 - 30 days.
- Unilateral complete cleft lip and alveolus.
- Presence of unilateral cleft palate.
- Medically free subjects.
- Both males and females.
Exclusion Criteria:
- Patients older than 30 days.
- Syndromic patients with other defects in addition to cleft lip and palate.
- Patients with bilateral cleft lip and palate.
- Incomplete Cleft lip.
- Medically compromised patients.
Sites / Locations
- Faculty of Dentistry
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
No Intervention
Experimental
Arm Label
Modified Nasoalveolar molding group
Taping group
Control group
CAD/NAM group
Arm Description
This group will receive nasoalveolar molding appliance in addition to taping for 3 Months with follow-up every 2 weeks.
Tape will be used alone in this group on the upper lip segments for 3 months with follow-up every 2 weeks.
This group will not receive any treatment.
Computer Aided Designed Nasoalveolar molding and 3D printed.
Outcomes
Primary Outcome Measures
Parents' satisfaction
It will be assessed using Questionnaire.
Secondary Outcome Measures
Nasal Esthetics: a- Nostril height
It will be measured in mm by Digital ruler on the images using a software.
Nasal Esthetics: b- Nostril width
It will be measured in mm by Digital ruler on the images using a software.
Nasal Esthetics: c- Nasal sill height
It will be measured in mm by Digital ruler on the images using a software.
Nasal Esthetics: d- Nostril area
It will be measured on the images in mm 2 (square) using a software measuring area.
Interlabial gap
It will be measured in mm by Digital ruler on the images using a software.
Maxillary Arch Dimension
It will be measured as distances in mm between landmarks identified on the dental models assessing the anterioposterior, transverse and vertical changes.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02845193
Brief Title
Effect of Novel Nasoalveolar Molding Techniques on Parents' Satisfaction and Short Term Treatment Outcomes in Unilateral Cleft Lip and Palate Infants: A Randomized Controlled Trial
Official Title
Effect of A Novel (Modified Grayson) Technique for Nasoalveolar Molding and Taping on Parents' Satisfaction and Short Term Treatment Outcomes in Infants With Unilateral Complete Cleft Lip and Palate: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
November 2016 (Actual)
Primary Completion Date
September 2018 (Actual)
Study Completion Date
April 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of this trial is to figure out the efficiency of modified Grayson NAM on parents' satisfaction, nasal esthetics, interlabial gap and maxillary arch changes. NAM might improve and facilitate the surgical procedure after lip closure. This might decrease the need of further interventions to improve esthetics and function of CLP patients. This trial will help the patients and practitioners in taking the decision of inclusion of NAM in the CLP treatment protocol as a mandatory step or skip a useless procedure with all of its burden.
Detailed Description
In this randomized trial, 4 groups will be included. The first group will receive a modified nasoalveolar molding appliance in addition to taping. In the second group, the patient will receive the CAD/NAM. the third group is tape only, while the fourth group remain untreated. the follow-up period will be 3 months till surgical lip closure. the assessment will be through a questionnaire for the parents' satisfaction outcome, photographs for nasal esthetics and interlabial gap outcome and maxillary models for the maxillary dimension change outcome.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cleft Lip and Palate
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
63 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Modified Nasoalveolar molding group
Arm Type
Experimental
Arm Description
This group will receive nasoalveolar molding appliance in addition to taping for 3 Months with follow-up every 2 weeks.
Arm Title
Taping group
Arm Type
Experimental
Arm Description
Tape will be used alone in this group on the upper lip segments for 3 months with follow-up every 2 weeks.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
This group will not receive any treatment.
Arm Title
CAD/NAM group
Arm Type
Experimental
Arm Description
Computer Aided Designed Nasoalveolar molding and 3D printed.
Intervention Type
Device
Intervention Name(s)
Modified Nasoalveolar molding
Intervention Description
Infants will receive this appliance which is a maxillary plate with nasal stent in addition to taping on the upper lip (taping is routine step in Grayson's nasoalveolar molding technique).
Intervention Type
Device
Intervention Name(s)
Taping
Intervention Description
Infants will receive a tape only on the upper lip segments to mold it to touch each other.
Intervention Type
Device
Intervention Name(s)
CAD/NAM
Intervention Description
computer aided design NAM
Primary Outcome Measure Information:
Title
Parents' satisfaction
Description
It will be assessed using Questionnaire.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Nasal Esthetics: a- Nostril height
Description
It will be measured in mm by Digital ruler on the images using a software.
Time Frame
3 months
Title
Nasal Esthetics: b- Nostril width
Description
It will be measured in mm by Digital ruler on the images using a software.
Time Frame
3 months
Title
Nasal Esthetics: c- Nasal sill height
Description
It will be measured in mm by Digital ruler on the images using a software.
Time Frame
3 months
Title
Nasal Esthetics: d- Nostril area
Description
It will be measured on the images in mm 2 (square) using a software measuring area.
Time Frame
3 months
Title
Interlabial gap
Description
It will be measured in mm by Digital ruler on the images using a software.
Time Frame
3 months
Title
Maxillary Arch Dimension
Description
It will be measured as distances in mm between landmarks identified on the dental models assessing the anterioposterior, transverse and vertical changes.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Days
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Infants with age range from 7 - 30 days.
Unilateral complete cleft lip and alveolus.
Presence of unilateral cleft palate.
Medically free subjects.
Both males and females.
Exclusion Criteria:
Patients older than 30 days.
Syndromic patients with other defects in addition to cleft lip and palate.
Patients with bilateral cleft lip and palate.
Incomplete Cleft lip.
Medically compromised patients.
Facility Information:
Facility Name
Faculty of Dentistry
City
Cairo
ZIP/Postal Code
00202
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
Yes
Learn more about this trial
Effect of Novel Nasoalveolar Molding Techniques on Parents' Satisfaction and Short Term Treatment Outcomes in Unilateral Cleft Lip and Palate Infants: A Randomized Controlled Trial
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