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A comparative pharmaco clinical study of kapikachhu and lata kasturi in shukra kshaya

A comparative pharmaco clinical study of kapikachhu ( mucuna prurita hook) and lata kasturi( hibiscus abelmoschus linn) in shukra kshaya ( oligospermia ) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090654
Enrollment
40
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: N538- Other male sexual dysfunction

Interventions

None listed

Sponsors

Pt Khushilal Sharma Govt Autonomous Ayurveda College Institute Bhopal madhya pradesh india
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Individuals aged between 21-50 years in male patient. 2.Semen test- sperm count less than 20million/ml. 3.Patients fulfilling the diagnostic criteria. 4.Individuals having clinical sign and symptoms of oligospermia according to Ayurvedic classics. 5.Individuals who will give written consent for the study.

Exclusion criteria

Exclusion criteria: 1.Aspermia patient/genital infection/congenital genital anamoly. 2.Individuals having any known systemic disorders like Cardiac disorders, Renal and Hepatic impairment, Diabetes Mellitus, Thyroid disorders and any type of Cancers. 3.Patient having past history of mumps.

Design outcomes

Primary

MeasureTime frame
It is expected that at the end of the study, we would be able to demonstrate the comparative efficacy of Kapikachhu (Mucuna prurita ) and Lata kasturi (Hibiscus abelmoschus) in Shukra kshaya (Oligospermia).Timepoint: 6 weeks

Secondary

MeasureTime frame
semen analysis for sperm countTimepoint: 6 weeks

Countries

India

Contacts

Public ContactDr Yogesh rathor

Pt Khushilal Sharma Govt Autonomous Ayurveda College Institute Bhopal

sharmavinod389@gmail.com9926379195

Outcome results

None listed

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