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A conceptual and applied study on lepa kalpana with special reference to efficacy of different modified lepa forms in primary dysmenorrhea

A CONCEPTUAL AND APPLIED STUDY ON LEPA KALPANA WITH SPECIAL REFERENCE TO EFFICACY OF DIFFERENT MODIFIED LEPA FORMS IN PRIMARY DYSMENORRHOEA - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088442
Enrollment
45
Registered
2025-06-09
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

None listed

Sponsors

Dr P VAISHNAVI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects coming under the age group of 12 to 35 years. 2.Subject with primary symptoms with or without secondary symptoms will be selected. 3.Subjects presenting with chief complaints of painful menstruation for at least 3 or more cycles. 4.Subject marital status with married and unmarried will be selected.

Exclusion criteria

Exclusion criteria: 1.Subjects with diagnosed other systemic disorders that interfere with study. 2.Secondary dysmenorrhea. 3.Subjects under oral and other contraceptive measures. 4.Subjects under other hormonal therapy. 5.Other diagnosed menstrual irregularities. 6.Lactating women. 7.Subjects diagnosed with PCOD. 8.Subjects with H/O pain after menstruation.

Design outcomes

Primary

MeasureTime frame
The modified lepa forms are anticipated to reduce the pain associated with primary dysmenorrheaTimepoint: At baseline, Every day during intervention-1/2/3/4 days (varies as duration of pain differs in each individual), After intervention 1/2/3/4 days (varies as duration of pain differs in each individual)

Secondary

MeasureTime frame
WaLIDD assessment score for dysmenorrhea reduction in gradeTimepoint: At baseline, Every day during intervention-1/2/3/4 days (varies as duration of pain differs in each individual), After intervention 1/2/3/4 days (varies as duration of pain differs in each individual)

Countries

India

Contacts

Public ContactDr P VAISHNAVI

Government Ayurveda Medical College and hospital mysuru

vachate37@gmail.com9448150212

Outcome results

None listed

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