Health Condition 1: N889- Noninflammatory disorder of cervixuteri, unspecified
Conditions
Interventions
Intervention1: Arm :1 : Mono therapy with Venpoosani nei (internal): 7.5 ml, Two times a day after food - Duration-40 days
Control Intervention1: Arm: 2 : Combination therapy with Venpoosani nei (inte
Sponsors
Central Council for Research in Siddha
Eligibility
Inclusion criteria
Inclusion criteria: 1 Age â?? 18 to 50 Years 2 Gender â?? Married Female 3 Thick whitish or yellowish or greenish discharge from vagina with foul smell 4 Itching and burning sensation in vulva 5 Vaginal swab test positive for micro-organism 6 Dysuria 7 Lower abdominal pain 8 Pain in lumbar region
Exclusion criteria
Exclusion criteria: 1.White discharge with bleeding 2.Ovarian cyst or tumor, prolapse 3.Pregnancy and lactation 4.Diabetes 5.Physiological vaginal discharge 6.Use of antibiotics or local vaginal formulation within the previous month
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Trial is to show vaginal swab negative for micro-organismTimepoint: After 40 days | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Reduction of signs and symptoms of vellai noi (leucorrhea) â?? (Severity score) 2.To assess whether administration of venpoosani nei alter the lipid levels by measuring lipid profile, before and after treatment. Timepoint: After 40 days | — |
Countries
India
Contacts
Public ContactDr P Sathiyarajeswaran
Siddha Central Research Institute
Outcome results
None listed