To study the clinical evaluation of bio specimen device
- Registration Number
- CTRI/2022/12/048267
- Lead Sponsor
- Iota Diagnostic Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Healthy Men and women volunteers are chosen in a ratio of 1:1 aged > 35 and
< 60years.
2.Subjects who are willing to participate in the study and sign the informed
consent document and comply with the trial procedure.
3.Having healthy skin on the test area as assessed by dermatological
examination and donâ??t have a history of allergy.
4.Subjects who are compliant with the study
1.Scars, excessive terminal hair, or tattoos on the studied area.
2.Dermatological infection/pathology on level of studied area.
3.Any clinically significant systemic or cutaneous disease, which may interfere
with study treatment or procedures.
4.Chronic illness which may influence the outcome of the study.
5.Subjects on any medical treatment either systemic or topical which may
interfere with the performance of the study treatment (presently or in the past
1 month).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method aboratory confirmation and analysis of the samples received from the clinical <br/ ><br>site.Timepoint: On first visit
- Secondary Outcome Measures
Name Time Method aboratory confirmation of the sample viability for different volumetric capacitiesTimepoint: On the visit