To Assess the functioning of Menstrual Fluid Collection Device- M- StripTM ?
Not Applicable
- Registration Number
- CTRI/2024/05/068173
- 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
Inclusion Criteria
1. Healthy women volunteers are chosen aged 30 to 55 years.
2. Subjects who are willing to participate in the study and sign the informed consent document and comply with the trial procedure.
3. Subjects who are compliant with the study
Exclusion Criteria
1. Pregnant and lactating women.
2. Clinical evidence of any serious systemic disease or acute illness, in the clinical opinion of the Investigator.
3. Subjects who are surgically sterile or have attained menopause (if they had their last menstruation more than 2 years back.
4. Subjects who were previously included or had participated in any other clinical study within 30 days prior to the date of consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method