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Effect of ayurvedic panchakarma (Trivrutta avaleha virechana) and Putranjivak seed powder on low sperm count (oligospermia): A clinical study

A Randomized Open Controlled Clinical trial to evaluate the efficacy of trivrutta avaleha virechana followed by Putranjivak beeja churna in ksheena shukra w.s.r. (oligozoospermia) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094944
Enrollment
68
Registered
2025-09-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: N461- Oligospermia

Interventions

None listed

Sponsors

Bhushan Appasaheb Kale
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Male patients aged between 20 and 50 years. Diagnosed case of Oligozoospermia Sperm count less than 15 million/ml Male patients who have signed for consent form Male patients fit for virechana karma.

Exclusion criteria

Exclusion criteria: Azoospermia. Congenital disorders related to reproductive system like bilateral absence of the vas deferens, cryptorchidism, marfans syndrome, Klinefelter s syndrome.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of trivrutta avaleha virechana followed by putranjivak beeja churna in ksheena shukra w.s.r. (oligozoospermia)Timepoint: 90 days

Secondary

MeasureTime frame
To compare the effect of trivrutta leha virechana followed by Putranjivak beeja churna over ashwatha phala churna in ksheena shukra (oligozoospermia)Timepoint: 90 days;To observe the efficacy of trivrutta leha virechana followed by Putranjivak beeja churna in ksheena shukra w.s.r. (oligozoospermia)Timepoint: 90 days;To achieve improvement in sperm count when given for 90 days.Timepoint: 90 days

Countries

India

Contacts

Public ContactBhushan Appasheb Kale

Department of PG studies in Prasuti tnatra and striroga, Yashwant Ayurvedic College A/p. Kodoli

vishalaturlapati@gmail.com9960217429

Outcome results

None listed

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