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Homoeopathy in the treatment of Premenstrual syndrome

Effectiveness of Individualized Homoeopathic Medicines in 50 millesimal potency for the treatment of Premenstrual Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041760
Enrollment
90
Registered
2022-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: N943- Premenstrual tension syndrome

Interventions

Intervention1: Individualized homoeopathic medicine in 50 millesimal potencies.: Each dose will be subdivided in dilute form for 16 days or 32 days, as per need of the case. Control Intervention1: Not

Sponsors

Dr Usha Ghelani Uchat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Female Patients of 18 to 40 years of age. 2. Patients from all religion and all socio-economic status 3. Participants had to fulfil the diagnostic criteria for Premenstrual syndrome. 4. Patients willing to do laboratory investigations when required for the study. 5. Patients willing to participate in the study of clinical work.

Exclusion criteria

Exclusion criteria: 1. Patients unwilling to participate in the study of clinical work. 2. Patients suffering from any psychiatric conditions, concomitant psychotherapy or alternative therapies used. 3. Alcohol or drug dependence. 4. Concomitant use of sex hormones. 5. Pregnant patients, patients who were breast feeding, and/or with likelihood of pregnancy. 6. Any symptoms suggestive of any serious medical conditions.

Design outcomes

Primary

MeasureTime frame
PMS SELF EVALUATION QUESTIONNAIRETimepoint: Baseline and 6 months

Secondary

MeasureTime frame
Any pathological condition of female genital organ associated with PMSTimepoint: Baseline and after 6 months

Countries

India

Contacts

Public ContactDr Usha Ghelani Uchat

National Institute of Homoeopathy

ushauchat@gmail.com9830966265

Outcome results

None listed

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