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A Clinical study to assess the Effectiveness of VISPO on Urinary Symptoms in Female Subjects.

Not Applicable
Conditions
Health Condition 1: N390- Urinary tract infection, site notspecified
Registration Number
CTRI/2022/10/046779
Lead Sponsor
Vidya Herbs Pvt Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Women with frequent urination, nocturia, and/or urgency for at least 2 months

2.Urinary symptoms that do not require medical treatment based on definitions by physicians

3.Must be able to read and understand in English or local language and maintain a subject diary

4.Must be willing and able to give informed consent and comply with the study procedures.

Exclusion Criteria

1.Suspected to have overactive bladder (OAB) according to the core lower urinary tract symptom score (CLSS) and the OAB symptom score (OABSS).

2.Currently receiving or have received treatments for urinary disorders within the past 2 months

3.Subjects who are unable to have the desire to urinate.

4.Subjects who have dysuria as the main symptom

5.Subjects allergic to herbal products or any component of the study product

6.History of uncontrolled chronic or lifestyle related disease

7. Known HIV or Hepatitis B positive or any other immuno-compromised state

8. Currently participating or having participated in another clinical trial during the last 3 months prior to the beginning of this study

9. Any additional condition(s) that in the Investigators opinion would warrant exclusion from the study or prevent the subject from completing the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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