PHARMACEUTICAL ANALYTICAL AND CLINICAL STUDY OF VANARI GUTIKA AND VANARI AVALEHA IN APHRODISIAC EFFECT

PHARMACEUTICO ANALYTICAL AND CLINICAL STUDY OF VANARI GUTIKA IN DIFFERENT DOSAGE FORMS WSR TO VAJIKARANA EFFECT

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/07/015060

Enrollment

Registered

2018-07-26

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- Shukrakshaya(oligospermia) Erectile dysfunction

Interventions

Intervention1: Vanari Gutika: Composition:Kaunch beej,Cow milk,Ghrita,Sharkara, Honey. Dose 10 gram twice a day route of administration orally duration 1 month Control Intervention1: Vanari Avleha:

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed and confirmed cases of Shukra kshaya (oligospermia) Erectile dysfunction etc on the basis of symptoms and laboratory investigations

Exclusion criteria

Exclusion criteria: Patients suffering from chronic infections and any other serious illnesses Patients suffering from any venereal disease All congenital and surgical cases of impotency

Design outcomes

Primary

Measure	Time frame
Subjective parameters: Dourbalya(Weakness) Mukhashosha(Dryness ofmouth) Pandu(Paleness) Sadana (Lethargy) ï?? Shrama (Tiredness/Fatigue) Timepoint: 0 and 30 days	—

Secondary

Measure	Time frame
Semen analysis â?? All parameters Blood test like â?? CBC RBS etc Timepoint: 0 and 30 days	—

Countries

India

Contacts

Public ContactDr Mohar Pal Meena

National Institute of Ayurveda Jaipur

drmpmeena73@gmail.com9414564382

Outcome results

None listed

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