To evaluate the effect of Palashaadi varti on abnormal vaginal discharges.

Evaluation of the Effect of Palashadi Varti in the Management of Shweta Pradar (Abnormal Vaginal Discharge) on Clinical & Microbiological Parameters

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/05/052519

Enrollment

200

Registered

2023-05-11

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient willing for the trial and ready to consent. 2. Married female patients/sexually active patients. 3. Patient complaining Shewtapradar(Abnormal Vaginal Discharge) as a major symptom. 4. Women of Reproductive Age Group between 20 to 45 years of age.

Exclusion criteria

Exclusion criteria: 1.Unmarried women 2.Pregnancy 3.Lactating 4.Menopausal 5.Certain Gynecological Pathologies like CA cervix , fibroid polyp etc. 6.HIV positive patients. 7.Diabetic 8. Severely Anemic patients.

Design outcomes

Primary

Measure	Time frame
Overall improvement in vaginal discharge, congestion, vaginal itching and cervical erosionsTimepoint: 14 days	—

Secondary

Measure	Time frame
The results of antibacterial study to prove the effectiveness of trial drug on specific bacteriaTimepoint: 1 and half year	—

Countries

India

Contacts

Public ContactDr Akshita

RGGPG Ayurvedic College and Hospital

skbhardwaj73@gmail.com9418499799

Outcome results