Clinical Trials Directory

Trials / Completed

CompletedNCT05738733

A Clinical Efficacy Study of MsChief Personal Lubricant in Healthy Female Subjects

A Proof of Science, In-Use Tolerance, Safety, and Efficacy Clinical Study of MsChief Personal Lubricant in Healthy Female Subjects

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
138 (actual)
Sponsor
NovoBliss Research Pvt Ltd · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

A Proof of Science, Open-Label, Single Centre, Four-Arm, In-Use Tolerance, Safety, and Efficacy Clinical Study of MsChief Personal Lubricant in Healthy Female Subjects. 30 subjects/product (33 subjects' enrolment/treatment) healthy non-pregnant/non-lactating females with an age of 18 - 65 years old. A total of up to 132 subjects (33 subjects/product) will be enrolled to get 120 completed subjects (30 subjects/product) in the study.

Detailed description

A sufficient number of healthy female subjects with an age group of 18 - 65 years old with a Nugent score ≤3 will be recruited/enrolled. The potential subjects will be screened as per the inclusion \& exclusion criteria only after obtaining written informed consent from the subjects. The subjects will be instructed to visit the facility as per the below visits * Visit 01 (Within 07 Days): Screening, Baseline evaluations * Visit 02 (Day 01): Enrolment \& Test Products usage phase start * Visit 03 (Day 16): Test Products usage ends, End of the study Subjects will be pre-screened by the screening department of NovoBliss Research. Subjects will be telephonically contacted by recruiting department prior to the enrolment visit. Subjects will be instructed during screening (prior to enrolment) not to use any other product for intimate washes, lubricant, or any other product during the study. Assessment of efficacy parameters will be done before test products usage on Day 1 and will be compared with after test products usage during Day 16 as listed below. 1. Gynaecological Assessments * Local irritation, pruritus, erythema, edema * Moisturizing effect - moisture, dryness, flaking, epithelial mucosa * Quality and odour of vaginal discharge * Vaginal pH measure using pH paper * Clinical symptoms associated with infections * Verbal rating scale (0-4 score)- Vaginal itching 2. Subjective Self-assessments * Perceived irritations - Burning, Itching, Stinging, Discomfort * Sexual activity (where appropriate) * VAS Scoring for Vaginal itchiness * Quality of life assessment 3. Microbiological Assessments • Nugents scoring

Conditions

Interventions

TypeNameDescription
DEVICEMsChief Classic Natural LubricantApply the desire amount of lubricant on the body to make it more sensitive.
DEVICEMsChief Ylang Ylang Natural LubricantApply the desire amount of lubricant on the body to make it more sensitive.
DEVICEMsChief Vanilla & Citrus Natural LubricantApply the desire amount of lubricant on the body to make it more sensitive.
DEVICEMsChief Tea & Peach Natural LubricantApply the desire amount of lubricant on the body to make it more sensitive.

Timeline

Start date
2023-03-02
Primary completion
2023-04-22
Completion
2023-05-30
First posted
2023-02-22
Last updated
2023-07-10

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT05738733. Inclusion in this directory is not an endorsement.