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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04150783
Other study ID # Pro00102005
Secondary ID R01DE028554
Status Recruiting
Phase
First received
Last updated
Start date November 1, 2019
Est. completion date June 2025

Study information

Verified date January 2024
Source Duke University
Contact Amy Walker
Phone 919-684-17325
Email amy.walker1@duke.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to use computers to simulate airflow in 3D construction of your nasal cavity generated from cone beam CT images. The results from computer simulations will help researchers identify the severity of cleft-induced nasal dysfunction and assess the impact of current treatment in restoring breathing function. The ultimate goal is to improve post-surgery outcomes to restore nasal breathing function to normal levels.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date June 2025
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Provide signed and dated informed consent form. - Willing to comply with all study procedures and be available for the duration of the study. - Male or female, aged =18 years of age. - Clinical diagnosis of unilateral cleft lip nasal deformity (uCLND) - Scheduled to undergo elective surgery for nasal obstruction - Scheduled to have a Cone Beam Computed Tomography (CBCT) as part of the pre- operative work-up for elective surgery. Exclusion Criteria: - Prior cleft rhinoplasty or septoplasty for correction of nasal obstruction - Pregnant women: A pregnancy test will be performed within 48 hours of baseline - Patients unable or unwilling to comply with study procedures outlined in protocol

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Surgical repair for nasal obstruction
Patient reported quality of life questionnaires

Locations

Country Name City State
United States Duke University Medical Center and affiliated practices Durham North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Duke University National Institute of Dental and Craniofacial Research (NIDCR)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Validation of computational fluid dynamics simulation with breathing measurement Percent agreement between computational fluid dynamics simulated nasal resistance and nasal resistance from rhinomanometry breathing measurement 6 months
Primary Validation of computational fluid dynamics simulation with in vitro experiment Percent agreement between computational fluid dynamics simulated nasal resistance and nasal resistance measurement from in vitro experiment of 3D printed plastic nasal replica 6 months
Primary Effectiveness of current surgery in restoring nasal function based on volumetric airflow Analysis of significant difference in volumetric airflow rate between pre-surgery and post-surgery data from computational fluid dynamics simulations of patient-specific 3D nasal models generated from cone-beam computed tomography images. 6 months
Primary Effectiveness of current surgery in restoring nasal function based on nasal resistance Analysis of significant difference in nasal resistance between pre-surgery and post-surgery data from computational fluid dynamics simulations of patient-specific 3D nasal models generated from cone-beam computed tomography images 6 months
Primary Effectiveness of current surgery in restoring nasal function based on nasal heat flux Analysis of significant difference in nasal heat flux between pre-surgery and post-surgery data from computational fluid dynamics simulations of patient-specific 3D nasal models generated from cone-beam computed tomography images. 6 months
Primary Effectiveness of current surgery in restoring nasal function based on nasal moisture flux Analysis of significant difference in nasal moisture flux between pre-surgery and post-surgery data from computational fluid dynamics simulations of patient-specific 3D nasal models generated from cone-beam computed tomography images. 6 months
Primary Anatomical sites of greatest nasal obstruction Analysis on agreement of computational fluid dynamics identified anatomical sites of greatest nasal obstruction from pre-surgery 3D nasal models and actual surgical anatomical sites. CFD identified sites of greatest nasal obstruction are regions in the airway with highest nasal resistance. 6 months
Primary Computational fluid dynamics based optimized treatment options for unilateral cleft lip nasal deformity patients based on volumetric airflow Creation of virtual surgery nasal airway models based on computational fluid dynamics identified anatomical sites of greatest nasal obstruction. Computational fluid dynamics generated unilateral left and right side percent asymmetric will be computed used to identify the top three virtual surgery nasal airway models with best treatment potentials for unilateral cleft lip nasal deformity patients 6 months
Primary Computational fluid dynamics based optimized treatment options for unilateral cleft lip nasal deformity patients based on nasal resistance Creation of virtual surgery nasal airway models based on computational fluid dynamics identified anatomical sites of greatest nasal obstruction. Computed nasal resistance will be used to identify the top three virtual surgery nasal airway models with best treatment potentials for unilateral cleft lip nasal deformity patients 6 months
Primary Computational fluid dynamics based optimized treatment options for unilateral cleft lip nasal deformity patients based on nasal heat flux Creation of virtual surgery nasal airway models based on computational fluid dynamics identified anatomical sites of greatest nasal obstruction. Computed nasal moisture flux will be used to identify the top three virtual surgery nasal airway models with best treatment potentials for unilateral cleft lip nasal deformity patients 6 months
Secondary Change in patient-reported outcome (PRO) measures Change PRO measures as measured by NOSE questionnaire baseline, 2 weeks, 8 weeks, 6 months, 12 months
Secondary Change in patient-reported outcome (PRO) measures Change PRO measures as measured by SCHNOS questionnaire baseline, 2 weeks, 8 weeks, 6 months, 12 months
Secondary Change in patient-reported outcome (PRO) measures Change PRO measures as measured by CLEFT-Q questionnaire baseline, 2 weeks, 8 weeks, 6 months, 12 months
Secondary in vitro analysis for top three virtual surgery nasal models with best treatment based on nasal pressure in vitro analysis from 3D printed plastic nasal replica of top three virtual surgery nasal models with best treatment potential will be done using unilateral airflow pressure. 6 months
Secondary in vitro analysis for top three virtual surgery nasal models with best treatment based on unilateral volumetric airflow in vitro analysis from 3D printed plastic nasal replica of top three virtual surgery nasal models with best treatment potential will be done using unilateral volumetric airflow rate. 6 months
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