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Dhatakyadi Varti-An Advance Therapy for Vulvovaginitis During Pregnancy

â??A CLINICAL STUDY ON UPAPLUTA YONIVYAPAD w.s.r. TO VULVOVAGINITIS DURING PREGNANCY & ITS MANAGEMENT WITH DHATAKYADI VARTIâ??

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/05/005747
Enrollment
60
Registered
2015-05-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

None listed

Interventions

Intervention1: TRIAL DRUG AND CLOTRIMAZOLE,CLINDAMYCIN VAGINAL SUPPOSITORIES: PATIENT WERE RANDOMLY DIVIDED IN TWO GROUPS.IN TRAIL GROUP DHATAKYADI VARTI(3G) WAS INSERTED LOCALLY IN VAGINA AT BED TI

Sponsors

IPGTRA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.The pregnant women with different parity having signs and symptoms of vulvovaginitis. 2.Age 19 to 40years. 3.White discharge present during examination. 4.Inflammation present in vulva and vagina. 5.Pathogens present in wet slide study and vaginal swab culture.

Exclusion criteria

Exclusion criteria: 1.Non pregnant Women. 2.Age below 19yrs or above 40 yrs 3.Hypersensitivity to drug and inability to conform the protocol. 4.Women with severe Physical illness, any systemic disease like D.M.,any organic Pathology, Hepatic, Cardiac, Renal disease and any acute Infection of any system, 5.Women suffering from disease like S.T.D.,H.I.V.etc.

Design outcomes

Primary

MeasureTime frame
PATIENT GOT SYMPTOMATIC RELIVE IN BOTH GROUPSTimepoint: AFTER 14 DAYS OF TREATMENT

Secondary

MeasureTime frame
TO PREVENT COMPLICATION LIKE PRE MATURE RUPTURE OF MEMBRANE AND PRE TERM LABORTimepoint: TO PREVENT COMPLICATION LIKE PRE MATURE RUPTURE OF MEMBRANE AND PRE TERM LABOR

Countries

India

Contacts

Public ContactDR SHILPA DONGA

MD (AYU)PHD

drshilpadonga@yahoo.com9825646796

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026