Clinical study to evaluate efficacy of Leuc syrup in leucorrohoea

Single Armed Clinical Study to Evaluate Efficacy Of Leuc Syrup in Leucorrohoea

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/02/049887

Enrollment

Registered

2023-02-20

Start date

Unknown

Completion date

Unknown

Last updated

2023-03-06

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

Conditions

Health Condition 1: - Health Condition 2: N771- Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Married women having age between 18 to 55 years. 2.Patients having any complaint of discharge per vagina, Itching sensation at vulva, Burning sensation in vagina, Pain in vagina, Foul smell from vagina , backache and pelvic pain.

Exclusion criteria

Exclusion criteria: 1.Female patients having pregnancy, breast feeding or post-delivery period. 2.Patients with any reproductive tract malignancy. 3.Patients with other systemic illness. 4.Patients with positive history of venereal diseases 5.Patients who are using CU-T or chemical method of contraception.

Design outcomes

Primary

Measure	Time frame
Relieve in white discharge per vaginaTimepoint: at base line , 14 days	—

Secondary

Measure	Time frame
White discharge per vaginaTimepoint: base line,14 days,4 weeks	—

Countries

India

Contacts

Public ContactNilofar Shaikh

JS Ayurveda Mahavidhyalaya

Shaikhnilofar12@gmail.com9638508994

Outcome results