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Homoeopathic Treatment Of Uterine Fibroid Using Epihysterinum

A Clinical Trial On The Efficacy Of Epihysterinum In The Treatment Of Uterine Fibroid

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052233
Enrollment
35
Registered
2023-05-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: D259- Leiomyoma of uterus, unspecified

Interventions

Intervention1: EPIHYSTERINUM 30/200/1M: Medicine will be given in 1 dose by oral route based on the follow up done at 15 days interval over a duration till the patient is not cured within 1 year of r

Sponsors

RBTS GOVT HOMOEOPATHIC MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Self reported and prediagnosed cases of Uterine Fibroids. Patients with symptomatology of Uterine Fibroids. Cases confirmed by USG or Laproscopy. Uterine fibroid of size less than 12 weeks

Exclusion criteria

Exclusion criteria: Patients or its guardian unwilling to take part or not giving consent to join the study. Diagnosed cases of systemic diseases psychiatric illness or other uncontrolled or life threatening illness affecting quality of life or any organ failure. Substance abuse and or dependence. Self reported immunecompromised state. Uterine Fibroid of size more than 12 weeks Persistent uterine bleeding despite medical therapy Excessive pain or pressure symptoms Recurrent pregnancy loss due to fibroid/or Rapidly growing myoma

Design outcomes

Primary

MeasureTime frame
Improvement in their symptomatology. Improvement in Aberdeen Menorrhagia Severity Scale(AMSS) score. Timepoint: 0-3 MONTHS

Secondary

MeasureTime frame
uterine fibroids Symptom and Quality of life UFSQOLTimepoint: 0-6 MONTHS

Countries

India

Contacts

Public ContactDR NIRBHAY KUMAR

RBTS Govt Hom Medical College and Hospital

drgkeshav.257@gmail.com8984681057

Outcome results

None listed

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