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Effect Of Ayurvedic Medicine In Piles.

Randomized Controlled Trial To Study The Efficacy of Patrakadi Vati In The Management of Abhyantar Arsha With Special Reference To First And Second Degree Internal Haemorrhoids. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082398
Enrollment
80
Registered
2025-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Sponsors

Gaurav Umesh Sachdev
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of age group 18 to 50 years. 2.Patients of both genders are accepted. 3.Patients diagnosed with Abhayantar Arsha [First and Second degree Haemorrhoids) will be selected. 4.Patients who provide written consent. 5.Individuals experiencing Haemorrhoidal symptom (pain, bleeding prolapse) for atleast 4 weeks.

Exclusion criteria

Exclusion criteria: 1.Patient with Haemoglobin less than 8gm%. 2.With known case of 3rd an 4th degree hemorrhoids,fissure,fistula,prolapsed rectum. 3.Patient with severe systemic illness such as HTN,Uncontrolled DM,CVD and HIV and Immunocompromised patients. 4.Pregnant And lactating mother. 5. Patients with active gastrointestinal disease Such as UC,CD,CA.

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is to assess the efficacy of oral administration of 250mg Patrakadi Vati with Gudodak twice daily for 28 days in managing Abhyantar Arsha (First and Second Degree Internal Hemorrhoids) by evaluating: Reduction in bleeding episodes, Improvement in constipation, Decrease in anal pain, Regression in pile mass size and number.Timepoint: 0,7th,14th and 28th Day

Secondary

MeasureTime frame
1.Duration of symptom relief (pain, constipation, pile mass regression) ,assessed on Day 7, Day 14, & Day 28. 2. Reduction in bleeding episodes measured by frequency & severity of hemorrhoidal bleeding on Day 7, Day 14, & Day 28. 3. Cost-effectiveness analysis comparison of healthcare expenses, treatment duration, & patient recovery time at the end of the study. 4. Objective improvements in hemorrhoidal size & number ,assessed via Proctoscopy on Day 0, Day 7, Day 14, & Day 28.Timepoint: Day 0th,7th,14th & 28th

Countries

India

Contacts

Public ContactDr Naimish Kishor Saraf

Siddhakala Ayurved mahavidyalay, Sangamner

naimishsaraf@gmail.com9766786123

Outcome results

None listed

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