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"study to compare Paribhadra and Nimba Pratisarniya Kshara in Internal Piles."

A Comparative Clinical Study To Evaluate The Efficacy Of Paribhadra Pratisarniya Kshara And Nimb Pratisarniya Kshara In The Management Of Abhyantara Arsha. - PANAA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105894
Enrollment
60
Registered
2026-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: K640- First degree hemorrhoids Health Condition 2: K641- Second degree hemorrhoids Health Condition 3: K642- Third degree hemorrhoids

Interventions

None listed

Sponsors

Shri Dhanwantri Ayurvedic Medical College And Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-Patients between the age of 20-60 years of either sex 2-Patients suffering from sign and symptoms of first,second,third degree of internal hemmorroids with or without other sign and symptoms 3-Patients with the sign and symptoms of arshas of pittaja and raktaja orijin 4-Arsha which are mrudu(soft),prasrutha(elaborated),avaghada(deep) and uchruta(projected) 5-Patients fit for kshara karma 6-Patients who will be ready to give written informed consent

Exclusion criteria

Exclusion criteria: 1-Grade fourth hemmorroids 2-Patients with thrombosed or prolapsed hemmorroids requiring emergency surgical intervention 3-Unconrolled diabetes/Hypertension 4-Patients having reactive viral markers(HBsAg,Anti-HCV,HIV) 5-Patients suffering from associated anorectal conditions(eg.fissure-in-ano,fistula-in-ano,carcinoma rectum) 6-Pregnant and lactating women 7-Patients not willing to paticipate or not ready to give written informed consent

Design outcomes

Primary

MeasureTime frame
Assessment of change in severity of symptoms of abhyantara arsha such as bleeding per rectum,pain and size of pile mass after 21 days of treatment Timepoint: Baseline(Day 0),Day 7,Day 14,Day 21(end of treatment) and follow-up on day 30.

Secondary

MeasureTime frame
Assessment of associated symptoms of abhyantara arsha such as itching,discharge and prolapse of pile mass along with overall improvement in patient conditions. Timepoint: Baseline(Day 0),Day 7,Day 14,Day 21(end of treatment) and follow-up on day 30.

Countries

India

Contacts

Public ContactPushpendra singh pal

Shri Dhanwantri Ayurvedic Medical College And Research Centre

tejo_lakshman@yahoo.co.in9618819276

Outcome results

None listed

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