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

NCT05738733 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 138

Last updated 2023-07-10

No results posted yet for this study

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.

Conditions

  • Healthy Females

Interventions

DEVICE

MsChief Classic Natural Lubricant

Apply the desire amount of lubricant on the body to make it more sensitive.

DEVICE

MsChief Ylang Ylang Natural Lubricant

Apply the desire amount of lubricant on the body to make it more sensitive.

DEVICE

MsChief Vanilla & Citrus Natural Lubricant

Apply the desire amount of lubricant on the body to make it more sensitive.

DEVICE

MsChief Tea & Peach Natural Lubricant

Apply the desire amount of lubricant on the body to make it more sensitive.

Sponsors & Collaborators

  • TTK Healthcare Ltd - Protective Devices Division

    collaborator UNKNOWN

  • NovoBliss Research Pvt Ltd

    lead OTHER

Principal Investigators

  • Dr Nayan K Patel, MBBS · Medical Director

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-03-02
Primary Completion
2023-04-22
Completion
2023-05-30

Countries

  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05738733 on ClinicalTrials.gov