Skip to content

The Study To assess The Effectiveness Of Homoeopathic Medicine Viburnum Opulus In Cases Of Pelvic Inflammatory Disease In Comparison To Individualized Medicines.

A Randomized Controlled Trial To Assess The Effectiveness Of Individualized Medicine As Compared To Individualized Medicine Along With Viburnum Opulus As An Add On Therapy In The Management Of Pelvic Inflammatory Disease

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043100
Enrollment
70
Registered
2022-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: N739- Female pelvic inflammatory disease, unspecified

Interventions

Intervention1: Individualized Homoeopathic Medicines: According to symptoms similarity 200ch or 1M 1dose or 2 dose 4 globules for 14 days according to patients susceptibility Control Intervention1: In
thin, yellowish white after menses. 2.Pain in ovarian region. 3.Bearing-down pains: in pelvic region,with uneasiness. 4.Menstrual pain. 5.Menses began ten days early (always regular before) 6.pain in

Sponsors

Dr MPK Homoeopathic Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Previously diagnosed cases of PID seeking homoeopathic treatment or newly diagnosed. 2. As per sign & symptoms and CDC (adopted from DC Duttaâ??s textbook of gynecology 7th edition) Patients with 3-4 confirmatory sign and symptoms given below shall be enrolled for the study irrespective of the diagnosis based on investigations- a. Pelvic pain or lower abdomen pain or back pain. b. Abnormal & heavy Vaginal discharge (purulent and or copious) c. Offensive vaginal odor. d. Cervical motion tenderness. e. Lower abdomen tenderness. f. Adnexal tenderness. g. Pruritis vulva. h. Burning. i. Dyspareunia. j. Irregular vaginal bleeding. k. Fever Diagnostic criteria- 1.symptoms as mentioned above. 2.USG/ laboratory investigation done if required in case of unclear symptoms given above.

Exclusion criteria

Exclusion criteria: 1. Cases which required any emergency treatment. 2. Patient pursuing other treatment and were not willing to leave it. 3. Pregnant women and lactating mothers will not be included in the study. 4.Immunocompromised patient such as suffering from HIV, Hepatitis B/C etc. 5.Cases with multi systemic illness will be excluded from the study and cases with advance pathology & malignancy.

Design outcomes

Primary

MeasureTime frame
Changes in VAS score will be noted for every symptom before, during and after treatment and shall be analysed to assess the efficacy of treatment given.Timepoint: Changes in VAS score will be noted for every symptom before, during and after treatment and shall be analysed to assess the efficacy of treatment given at 12 month.

Secondary

MeasureTime frame
Changes in WHO QOL-BREF scale will be noted for before and after treatment and shall be analysed to assess the efficacy of treatment given .Timepoint: 1year

Countries

India

Contacts

Public ContactDr Ankita Srivastava

Dr MPK Homoeopathic Medical College Hospital And Research Centre Homoeopathy University

drvanijasharma@gmail.com9680438770

Outcome results

None listed

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