To study the effects gunjadi varti and ghoshaphala varti in the treatment of bleeding piles.(Abhyantar guda arsha)

A clinical control study of gunjadi varti and ghoshaphala varti in the management of abhyantar guda arsha (2nd degree haemorrhoid) - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/092101

Enrollment

Registered

2025-07-31

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

Health Condition 1: K641- Second degree hemorrhoids

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient having 2nd degree haemorrhoids. 2.Selection of patient will be done irrespective of sex ,religion and socioeconomic class.

Exclusion criteria

Exclusion criteria: 1)Patient having 3rd & 4th degree haemorrhoids. 2)Patient having CA Rectum & anal canal. 3)Pregnancy. 4)Patient having DM, HTN, HIV, HBsAG, Tuberculosis or any other systemic disorder.

Design outcomes

Primary

Measure	Time frame
Efficacy of Gunjadi Varti and Ghoshaphala Varti in reducing key symptoms of abhyantar guda arsha (2nd degree haemorrhoids) over a period of 28 days, assessed both subjectively and objectively. Subjective parameters: Vedana(pain) Toda(pricking pain) Kandu(itching) Malavbaddhata(constipation) Colour of pile mass Objective criteria: Number of arshankur(haemorrhoids) Bleeding. Timepoint: Weekly upto 28 days	—

Measure

Time frame

Efficacy of Gunjadi Varti and Ghoshaphala Varti in reducing key symptoms of abhyantar guda arsha (2nd degree haemorrhoids) over a period of 28 days, assessed both subjectively and objectively. Subjective parameters: Vedana(pain) Toda(pricking pain) Kandu(itching) Malavbaddhata(constipation) Colour of pile mass Objective criteria: Number of arshankur(haemorrhoids) Bleeding. Timepoint: Weekly upto 28 days

—

Secondary

Measure	Time frame
Overall symptom relief grading Excellent greater than 75 percent relief Marked 41 to 75 percent Moderate 25 to 50 percent Mild less than 25 percent Safety & tolerability Any adverse effects or withdrawal due to side effects Comparative effectiveness to determine which formulation is more effective clinically & objectivelyTimepoint: Weekly upto 28 days	—

Countries

India

Contacts

Public ContactDr Vishal Tamhane

Ashvin Rural Ayurved College and Hospital, Sadhvi Preetisudhaji Maharaj Nagar, Manchi Hill, Ashvi Bk, Tal.Sangamner, Dist.Ahmadnagar

vtamhane@gmail.com9764139607

Outcome results