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A Clinical Trial of Kusthadi Yonivarti in Cervical Erosion

A clinical study to evaluate the efficacy of Kusthadi varti in Karnini Yoni Vyapad (Cervical Erosion)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046307
Enrollment
30
Registered
2022-10-10
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: N86- Erosion and ectropion of cervix uteri

Interventions

None listed

Sponsors

Raihana Ahmed Choudhury
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: DEGREE OF CERVICAL EROSION,CERVICAL EDEMA, DISCHARGE FROM VAGINA,ITCHING,LOWER ABDOMINAL PAIN,LOW BACK ACHE, BLEED ON TOUCH

Exclusion criteria

Exclusion criteria: 1.PRAGNENT LADY 2.HIV,HBsAG,STD,FUNGAL INFECTION,MALIGNANCY,AUB, DUB. 3.PATIENT SUFFERING FROM ANY SYSTEMIC DISEASE 4.SYMPTOMS ASSOCIATED WITH UNDERLYING PELVIC PATHOLOGY LIKE UTERINE FIBROID, OVARIAN CYST,PID.

Design outcomes

Primary

MeasureTime frame
decrease in symptoms of karnini yonivyapad(cervical erosion)like 1.Reducing degree of cervical erosion. 2.reducing cervical edema 3.reducing discharge per vagina and itching 4.minimizing lower abdominal pain 5.reducing low back ache Timepoint: 2 weeks ,4 weeks

Secondary

MeasureTime frame
vaginal PH will be within normal range Healthy state of cervix on Per Speculum examination Normal urine Routine and No growth of microorganisms on Culture sensitivity examination.Timepoint: 30 days

Countries

India

Contacts

Public ContactProf Dr Yanbeni Humtsoe

Govt Ayurvedic College and Hospital,Guwahati, Assam

pybeni17@gmail.com8638807437

Outcome results

None listed

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