Clinical Trials Directory

Trials / Completed

CompletedNCT02363465

Echographic Measurement of Skin Thickness

Echographic Measurement of Skin Thickness at the Deltoid and Proximal Forearm in Adults

Status
Completed
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
Novosanis NV · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

To optimize a medical device for intradermal injection, knowledge concerning the thickness of epidermis and dermis at the proximal forearm is required. Since scientific knowledge is lacking, the investigators will examine the skin thickness (epidermis and dermis) of adults using imaging technology (High Frequency Ultrasound). The investigators hypothesize that they are able to correlate the thickness of the (epi)dermis to a specific combination of parameters age, gender, and BMI. Based on these results, the investigators can define which needle type and length is needed to correctly perform injections into the dermal layer.

Conditions

Interventions

TypeNameDescription
OTHEREchographic measurement of skin thickness(Epi)Dermal thickness at the proximal forearm and the deltoid region will be measured using imaging technology, more specifically high-frequency ultrasound (20-40 MHz) in B-mode (VEVO 2100®, Visual Sonics). This non-invasive measuring technique has already been proven to be accurate. The echographic measurement will be performed on the left and right deltoid region and on two sides of the proximal forearm. Both the dorsal part and the volar/palmar part of the proximal forearm will be investigated. Ultrasound will be executed using gel (Aquasonic®) to optimize imaging.

Timeline

Start date
2015-01-01
Primary completion
2015-06-01
Completion
2015-06-01
First posted
2015-02-16
Last updated
2015-10-06

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02363465. Inclusion in this directory is not an endorsement.