To evaluate the efficacy of Vrishya Gutika in the management of erectile dysfunction.

Clinical study on erectile dysfunction in male and its management with Vrishya Gutika - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086149

Enrollment

100

Registered

2025-05-02

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: N529- Male erectile dysfunction, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Male patients aged between 25 to 60 years

Exclusion criteria

Exclusion criteria: 1.Patient below 25 or above 60 year of age. 2.Spinal cord injury patients 3.ED secondary to medication (corticosteroids, antipsychotic, antidepressant, antandrogenic therapy etc) 4.Patients suffering from major systemic illness DM/HTN/Cancer/ HIV/Thyroid disease etc. 5.Have an IIEF-EF domain score of greater than or equal to 26 at screening 6.Active lesion or infection in penile or pubic area. 7.H/o hypersensitivity to any of the trial drugs or their ingredients.

Design outcomes

Primary

Measure	Time frame
To study the efficacy of Vrishya Gutika in the symptomatology of erectile dysfunction of male.Timepoint: 60 days	—

Secondary

Measure	Time frame
To study the efficacy of Vrishya Gutika in the management of erectile dysfunction according to IIEF scale.Timepoint: 3 weeks, 6 weeks, 9 weeks.	—

Countries

India

Contacts

Public ContactDr Manir Uddin Dewan

Govt. Ayurvedic College and Hospital Guwahati 781337

dr.manir@gmail.com9864174788

Outcome results