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Management of Chronic Cervicitis by Oral administration of Tablet Triphala Guggulu and Yoni Pichu with Darvi Taila

Phase 2
Conditions
Health Condition 1: N72- Inflammatory disease of cervix uteri
Registration Number
CTRI/2024/03/064419
Lead Sponsor
Faculty of Ayurveda Institute of Medical Sciences BH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Only married women of different age group and parity.

2. Patients presenting with at least any 3 of the following clinical signs and symptomatology

of chronic Cervicitis like -

a. Patients presenting with mucopurulent discharge p/v and endocervical bleed.

b. Patients having inflammatory Cervical Pap smear.

c. Patients presenting with clinical features of dyspareunia and cervical tenderness.

d. Patients presenting with clinical features of cervical congestion /strawberry cervix.

e. Patients presenting with intermenstrual/ post coital bleeding.

f. Patients presenting with other symptoms of cervicitis like back ache and lower

abdominal pain.

Exclusion Criteria

1. Unmarried

2. Pregnant women and Patients suffering from any specific organic lesions such as

Tuberculosis, acute or chronic respiratory diseases, cardiac diseases, renal diseases,

Diabetes mellitus, Hypertension etc.

3. Women with carcinoma of cervix, benign or malignant growth of reproductive tract, any

degree of genital prolapses.

4. Patients having their HIV and VDRL reactive.

16

5. Patients with Cervical Pap smear showing either CIN or papilloma virus infection or

invasive malignancy.

6. Patients having Acute cervicitis.

7. Patients having Acute Pelvic inflammatory disease.

8. Patients with h/o surgery of cervix.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Based on Subjective and Objective criteria and Laboratory investigations <br/ ><br>Subjective criteria: <br/ ><br>? Vaginal discharge <br/ ><br>? Post coital bleeding <br/ ><br>? Back ache <br/ ><br>? Inter menstrual spotting <br/ ><br>? Dyspareunia <br/ ><br>Objective criteria: <br/ ><br>? Cervical Congestion <br/ ><br>? Cervical discharge <br/ ><br>? Vaginal discharge <br/ ><br>? Cervical tenderness <br/ ><br>? Contact bleeding <br/ ><br>Laboratory investigations <br/ ><br>? Positive inflammatory Pap smear <br/ ><br>? Positive endocervical swab culture <br/ ><br>? ColposcopyTimepoint: 3 Follow ups with equal interval of 15 days
Secondary Outcome Measures
NameTimeMethod
Reduced inflammation ,alleviated symptoms and improved quality of life among study participantsTimepoint: 3 follow ups with Regular interval of 15 days.2 follow ups with medication and 1 follow up without medication
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