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Studying the Role of Homoeopathic Medicines in Reducing Premenstrual Symptoms in Women

Efficacy of individualised homoeopathic medicines in the treatment of premenstrual syndrome assessed by premenstrual syndrome scale (PMSS) -a quasi-experimental time series design. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090698
Enrollment
55
Registered
2025-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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.: individualized homoeopathic medicines prescribed based on the totality of the symptoms. Route- Oral, Dose- 4 pills-one dose followed by Placebo-

Sponsors

Dr Silaiezhil M
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Diagnosed subjects of Premenstrual Syndrome (PMS) as per American College of Obstetrician and gynecology practice bulletin 2001 criteria. 2) Subjects who are voluntarily willing to participate and sign the written informed consent

Exclusion criteria

Exclusion criteria: 1) Subjects who are on contraceptive pills or any other medications for Premenstrual Syndrome (PMS) 2) Women who are already on Psychiatric medications for depression, anxiety, schizophrenia or any other psychiatric illness. 3) Subjects who are a Known case of PCOD/ Hypothyroidism. 4) Subjects having uterine /ovarian/ pelvic pathology assessed with sonography of pelvis or transvaginal scan.

Design outcomes

Primary

MeasureTime frame
Change in PMSS (Premenstrual Syndrome Scale) total score from baseline (Month 3) to end of treatment (Month 6).Timepoint: 3 years

Secondary

MeasureTime frame
NIlTimepoint: NIl

Countries

India

Contacts

Public ContactDr Silaiezhil M

SJPEs Homeopathic Medical College and Hospital

hmc_h@yahoo.com7218677677

Outcome results

None listed

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