| CTRI Number |
CTRI/2026/02/103821 [Registered on: 13/02/2026] Trial Registered Prospectively |
| Last Modified On: |
|
| Post Graduate Thesis |
No |
| Type of Trial |
Interventional |
|
Type of Study
|
Other (Specify) [Clinical Safety and Efficacy Study] |
| Study Design |
Single Arm Study |
|
Public Title of Study
|
Consumer study for face serum. |
|
Scientific Title of Study
|
A Consumer Insight Study with Instrument-Based Evaluations of Glow Pro and The Glow Threads Silk Peptide Face Serum in Healthy Adult Female Participants. |
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NB260004-ST |
Protocol Number |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Nayan Patel |
| Designation |
Principal Investigator |
| Affiliation |
NovoBliss Research Pvt. Ltd. |
| Address |
313 Silver Radiance 4, Gota
Ahmadabad GUJARAT 382481 India |
| Phone |
07948983895 |
| Fax |
|
| Email |
dr.nayan@novobliss.in |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Nayan Patel |
| Designation |
Principal Investigator |
| Affiliation |
NovoBliss Research Pvt Ltd. |
| Address |
313 Silver Radiance 4, Gota
Ahmadabad GUJARAT 382481 India |
| Phone |
07948983895 |
| Fax |
|
| Email |
dr.nayan@novobliss.in |
|
Details of Contact Person Public Query
|
| Name |
Maheshvari Patel |
| Designation |
Director Operations and Strategic Management |
| Affiliation |
NovoBliss Research Pvt. Ltd. |
| Address |
313 Silver Radiance 4, Gota
Ahmadabad GUJARAT 382481 India |
| Phone |
07948983895 |
| Fax |
|
| Email |
maheshvari@novobliss.in |
|
|
Source of Monetary or Material Support
|
| Skintouch Beauty Private Limited - 312, Shivalik Satyamev, Nr. Vakil Bridge,
Sardar Patel Ring Rd, South Bopal
Bopal, Ahmedabad-380058, Gujarat-India
|
|
|
Primary Sponsor
|
| Name |
Skintouch Beauty Private Limited |
| Address |
312, Shivalik Satyamev, Nr. Vakil Bridge,
Sardar Patel Ring Rd, South Bopal
Bopal, Ahmedabad-380058, Gujarat-India
|
| Type of Sponsor |
Other [Wholesale N.E.C] |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Nayan Patel |
NovoBliss Research Pvt Ltd |
313, Silver Radiance-4, Gota Ahmadabad GUJARAT |
07948983895
dr.nayan@novobliss.in |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| ACEAS - Independent ethics committee |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Healthy Human Volunteers |
Healthy female volunteers |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
Glow Pro + The Glow Threads Silk Peptide Face Serum |
Mode of Usage: Participant will be instructed to cleanse the face and neck thoroughly and gently pat dry prior to product application. An adequate amount of The Glow Threads Silk Peptide Face Serum will then be applied evenly to the face. Following serum application, the Pro Touch Glow Pro device will be switched on by long-pressing the power button. Using the same button, participants will select MC Mode on high intensity for use. The device will then be gently glided over the face and neck area in accordance with the recommended usage instructions.
Frequency: Once a Day; as & when required
Storage temperature: Store at room temperature 20°C to 30°C, away from sunlight
Application Site: Face and Neck
Marketed By: Skintouch Beauty Pvt Ltd
Route of Application: Topical |
| Comparator Agent |
Nil |
NA |
|
|
Inclusion Criteria
|
| Age From |
22.00 Year(s) |
| Age To |
42.00 Year(s) |
| Gender |
Female |
| Details |
1) Age: 22-42 years old (both inclusive) female consumers.
2) Sex: Healthy male and non-pregnant/non-lactating female.
3) Females of childbearing potential must have a self-reported negative urine pregnancy test.
4) Subject is in good general health as determined by the Investigator on the basis of medical history.
5) Consumers should be willing and able to follow the study protocol to participate in the study.
6) Subject must be able to understand and provide written Subject’s information sheet to participate in the study.
7) Consumers is willing not to use any other marketed product on application site during the study period.
|
|
| ExclusionCriteria |
| Details |
1) Subject has any known allergy to test product ingredient.
2) Presence of any chronic disease or illness in the past three months or any clinically significant on-going chronic medical illness e.g. Congestive cardiac failure, Hepatitis, Hypotensive episodes, etc.
3) Participation in any similar consumer study within the past 90 days.
4) Currently using any topical medications.
5) Any exceptions to the inclusion/exclusion criteria will be considered on a case-by case basis and will be documented in the case report form
|
|
|
Method of Generating Random Sequence
|
Not Applicable |
|
Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Not Applicable |
|
Primary Outcome
|
| Outcome |
TimePoints |
To assess the effect of the test product in:
1. Skin lifting and firming using Cutometer® Dual MPA 580 by R2 and R7 parameters.
2. Skin hydration level by using Corneometer® CM 825.
3. Skin lifted appearance by using Visioface® RD
4. In terms of consumer perception for skin glow, serum absorption and puffiness reduction through 5-point Likert scale |
From the baseline before test product usage and after test product usage at T0 (+15) mins |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| NIL |
NA |
|
|
Target Sample Size
|
Total Sample Size="15" Sample Size from India="15"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
23/02/2026 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="0" Months="0" Days="1" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
This is an open-label, prospective, single-centre, consumer in-sight and instrumental evaluation study designed to evaluate the Glow Pro + The Glow Threads Silk Peptide Face Serum with respect to skin lifting and firming, hydration level, and lifted appearance following test product usage. The study population will include 15 adult female participants aged 22–42 years (both inclusive). All assessments will be conducted on a single study day at baseline, pre-usage of the test product and at T0 (+15) mins post usage of the test product. Assessments of the test product will be done as mentioned below: · Skin Lifting and Firming - Cutometer® Dual MPA 580 (R2 and R7) · Skin Hydration Level - Corneometer® CM 825 · Skin Lifted Appearance - Visioface® RD · Consumer perception regarding the skin glow, serum absorption, puffiness reduction through 5-point Likert Scale |