Health Condition 1: null- Patients having signs and symptoms of Cervicitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.All married women having signs and symptoms of Cervicitis- Mucopurulent vaginal discharge,Reddened and swollen cervix,Dyspareunia,Pruritis vulvae,Lower abdominal pain,frequent and painful micturition 2.Patient who will not use vaginal product during entire study. 3.Patient who will avoid sexual intercourse during entire study. 4.Patient who will follow the protocol. 5.Patients in which cervicitis is confirmed by pap smear test
Exclusion criteria
Exclusion criteria: Unmarried patients Any pathology of genital organs other than Cervicitis. Suspected pregnancy at screening or actively seeking pregnancy during study period. Serious underlying condition such as HIV or other primary or secondary immunosuppressive condition. H/O PID, ectopic pregnancy. Nursing mothers Psychiatric Patients Patients using hormonal preparation. Any specific or systemic diseases. Unable to follow the protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complains- Vaginal discharge, dyspareunia, bleeding during coitus, backache, lower abdominal pain Sign- Cervical size, congestion, consistency, inflammation Investigation- Pap smear Timepoint: Total four follow ups will be done at 15 days interval, out of which 3 will be with medication and 4th will be without medication | — |
Secondary
| Measure | Time frame |
|---|---|
| Routine- CBC with ESR, Urine-R/M, FBS, HIV, VDRL Specific- Pap Smear, Urine- C/S, USG, HVS- C/S Timepoint: 45 days | — |
Countries
India
Contacts
Banaras Hindu University