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Role of Homoeopathic Medicine in the treatment of pain during menses in young females

Effect of Lippes Keynotes and Red line Symptoms of the Materia Medica in Keynote Prescription for Primary Dysmenorrhea in Young Females: A Prospective Single Arm Clinicals Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077645
Enrollment
35
Registered
2024-12-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: N944- Primary dysmenorrhea

Interventions

Intervention1: Homoeopathic Medicine: Oral route of administration pill form 30 number pill size Centesimal scale First dose after case taking and subsequent doses after each follow up Potency acc

Sponsors

Bakson Homoeopathic Medical College And Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants with primary dysmenorrhea scoring more than 1 in WaLIDD score. Participants who are under the age group of 12 – 25 years of age. Participants with pain only during menstruation; with minimum of 3 cycles. Participants having poor sleep quality during menstrual cramp.

Exclusion criteria

Exclusion criteria: Participants who are suffering with any systemic or psychiatric or endocrine illness or under substance abuse or immunocompromised. Participants who are under any sort of treatment. Participants with known history of pathological pelvic conditions. Participants who refuse to give the consent.

Design outcomes

Primary

MeasureTime frame
It is expected that the scores in WaLIDD be will improved at the end of treatment, highlighting the benefits of Lippe’s keynotes and red line symptoms of the Materia Medica Timepoint: WaLIDD scale will be evaluated at baseline, 12th week, 24th weeks 15 months study Enrolment period 6 months Follow ups 6 months Data analysis and report writing 3 months

Secondary

MeasureTime frame
It is expected that the scores in PSQI be will improved at the end of treatment, highlighting the benefits of Lippe’s keynotes and red line symptoms of the Materia Medica. Timepoint: PSQI scale will be evaluated at baseline, 12th week, 24th week 15 months study Enrolment period 6 months Follow ups 6 months Data analysis and report writing 3 months

Countries

India

Contacts

Public ContactDr Ashwini Nair

Bakson Homoeopathic Medical College and Hospital

preeti.laroia@gmail.com9312352020

Outcome results

None listed

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