Ignite Creation Date:
2024-07-17 @ 11:04 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06489418
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-05
First Post:
2024-06-28
Brief Title:
A Clinical Study to Assess the Safety and Effectiveness of Test Product in Healthy Adult Human Subjects With Dry and Sensitive Skin
Sponsor:
NovoBliss Research Pvt Ltd
Organization:
NovoBliss Research Pvt Ltd
Study Overview
Official Title:
A Prospective Control-arm Site Randomized Evaluator-blinded Single-centre Safety and Efficacy Study of Test Product Dew Restore Barrier Repair Cream in Healthy Adult Human Subjects With Dry and Sensitive Skin
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
A prospective control-arm site randomized evaluator-blinded single-centre safety and efficacy study of Test Product Dew Restore Barrier Repair Cream in healthy adult human subjects with dry and sensitive skin
Detailed Description:
A total of 27 Subjects will be enrolled to complete 25 Subjects the study The potential subjects will be screened as per the inclusion exclusion criteria only after obtaining written informed consent from the subjects Subjects will be pre-screened by the screening department of NovoBliss Research Subjects will be called telephonically by the recruiting department prior to the enrolment visit Subjects will be told during screening prior to enrolment not to wear any facial make-up on the study visit day The adult female subjects will be instructed to visit the facility as per the below visits
Visit 01 Day 01 Screening Enrolment Baseline Evaluation On Site Product Usage Post Usage Evaluation
Visit 02 Day 02 Evaluations Product usage period
Visit 03 Day 15 2 Days Product Usage Period Evaluations
Visit 04 Day 30 2 Days Evaluations End of Study
Visit 01 Day 01 Screening Enrolment Baseline Evaluation On Site Product Usage Post Usage Evaluation
Visit 02 Day 02 Evaluations Product usage period
Visit 03 Day 15 2 Days Product Usage Period Evaluations
Visit 04 Day 30 2 Days Evaluations End of Study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None