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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05188235
Other study ID # 21-01096
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 10, 2022
Est. completion date December 2023

Study information

Verified date February 2023
Source NYU Langone Health
Contact Pablo Castaneda, MD
Phone (212) 598-6624
Email Pablo.Castaneda@nyulangone.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to collect data that will be used to later design a method for the early diagnosis of diagnosis of developmental dysplasia of the hip (DDH).


Description:

This will be a prospective study using an acoustic listening technique in combination with a standard clinical examination of DDH. For both the clinical cases and healthy children that are enrolled, that all subjects will have an ultrasound completed for comparison to the use of the studied tuning fork method. The gold standard is POCUS (point of care ultrasound as performed by the pediatric orthopedic surgeon). Collected data will be compared to POCUS as performed by an expert and this is standard of care. Healthy subjects will be referred for evaluation and found to be healthy on subsequent US.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Day to 6 Months
Eligibility Inclusion Criteria: - Infants included in this study must be born at full term with a gestational age of 0-6 months - Infants of both genders will be included - Infants must have been screened for DDH. Exclusion Criteria: - Infants born prematurely - Infants greater than six months of age. - Nonviable neonates and neonates of uncertain viability

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Acoustical Resonance Device
Infants will be studied for 15 min using an electronic "tuning fork" to transmit sound through the hip from a point on the skin while transmitted sounds FDA-approved stethoscope

Locations

Country Name City State
United States NYU Langone Health New York New York

Sponsors (2)

Lead Sponsor Collaborator
NYU Langone Health University of Central Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in soundwaves on the Actuator on patella, sensor on sacrum Descriptive statistics will be used to evaluate sound wave characteristics in infants with healthy hips. Inferential statistics will be used to compare the relationship between soundwave characteristics and diagnostic findings Study visit 1 (Day 1)
Primary Difference in soundwaves on the Actuator on patella, sensor on anterior superior iliac crest of pelvis Descriptive statistics will be used to evaluate sound wave characteristics in infants with healthy hips. Inferential statistics will be used to compare the relationship between soundwave characteristics and diagnostic findings Study visit 1 (Day 1)
Primary Difference in soundwaves on the Actuator on greater trochanter, sensor on sacrum Descriptive statistics will be used to evaluate sound wave characteristics in infants with healthy hips. Inferential statistics will be used to compare the relationship between soundwave characteristics and diagnostic findings Study visit 1 (Day 1)
Primary Difference in soundwaves on the Actuator on greater trochanter, sensor on anterior superior iliac crest Descriptive statistics will be used to evaluate sound wave characteristics in infants with healthy hips. Inferential statistics will be used to compare the relationship between soundwave characteristics and diagnostic findings Study visit 1 (Day 1)
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