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临床试验/CTRI/2025/11/098000
CTRI/2025/11/098000尚未招募2 期

A CLINICAL STUDY TO ASSESS THE EFFICACY OF EPIPHEGUS VIRGINIANA 30C IN REDUCING MIGRAINE - RELATED DISABILITY USING THE MIDAS SCALE

Dr Sanha1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年1月13日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
36
试验地点
1

研究概览

简要总结

Null Hypothesis:

Epiphegus Virginiana 30C has no significant effect on reducing migraine-related disability as measured by the MIDAS Scale.

Alternative Hypothesis:

Epiphegus Virginiana 30C significantly reduces migraine-related disability as measured by the MIDAS Scale.

Aim:

The aim of this study is to evaluate the efficacy of Epiphegus Virginiana 30C in reducing migraine-related disability, as measured by the MIDAS (Migraine Disability Assessment) Scale.

Objectives:

To assess the effectiveness of Epiphegus Virginiana 30C in the management of migraines.

To measure improvements in migraine-related disability using the MIDAS Scale.

Source of Data:

Study participants will be recruited from the OPD (Outpatient Department), peripheral OPD, and IPD (Inpatient Department) of A.M. Shaikh Homoeopathic Medical College, Hospital, and Post Graduate Research Centre, Belagavi.

Type of Research:

This is a prospective interventional single-arm clinical study.

Sampling Technique and Method:

The study will use a purposive, non-probability sampling method.

Selection Criteria:

Participants will be selected based on criteria supported by the International Headache Society (IHS).

Duration of Study:

All selected subjects will be enrolled within 15 months.

Tools Used in Study:

Standard case proforma.

Informed consent form.

MIDAS Questionnaire to assess migraine-related disability.

Inclusion Criteria:

Participants aged 18–60 years.

Diagnosed with migraine and having a history of the condition.

Exclusion Criteria:

Patients with headaches other than migraine.

Those currently undergoing long-term allopathic migraine treatment or using other anti-migraine medications.

Remedy Prescription Criteria:

All 36 cases will be treated with Epiphegus Virginiana 30C, prescribed according to the acute or sector totality of the case.

Follow-Up:

Follow-up will be conducted every month for a period of 3 to 6 months, based on the requirements of the individual case.

Result Criteria:

An improvement will be defined as a reduction of 10 or more points in the MIDAS score, indicating a significant decrease in migraine-related disability.

This study aims to assess whether Epiphegus Virginiana 30C offers a viable homeopathic treatment option for reducing the impact of migraines on daily functioning.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients of age groups between 18-60 years.
  • Pre-diagnosed cases of migraine with history.

排除标准

  • Cases of headache other than migraine.
  • Patients who are under any other medications for migraine (e.g., long-term prophylactic anti-migraine allopathic treatment).

研究者

发起方
Dr Sanha
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr. Sanha

AM Shaikh Homoeopathic Medical College And Hospital Belgaum

研究点 (1)

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