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Study comparing two treatment methods for patients with hemorrhoids (piles) using finger-guided hemorrhoidal artery ligation, with and without Apamarga Kshara application, to assess relief in hemorrhoid symptoms.

A Comparative Clinical Evaluation of Finger-Guided Hemorrhoidal Artery Ligation (FGHAL) With and Without Apamarga Kshara Lepa in Arsha (Hemorrhoids) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/111247
Enrollment
40
Registered
2026-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

None listed

Sponsors

Naveen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient identified with 2ND Degree, 3RD Degree and 4th Degree haemorrhoids (Arsha). 2. Age range: 18 to 60 years, inclusive of both genders. 3. Individuals who have provided written informed consent to take part in the study. 4. Patients not undergoing any additional simultaneous treatment for haemorrhoids throughout the study duration

Exclusion criteria

Exclusion criteria: 1. Patient with first-degree haemorrhoids. 2. Existence of any other ano rectal diseases like rectal prolapse, fistula-in-ano, fissure-in-ano, or perianal abscess. 3. Individuals with bleeding disorders or undergoing anticoagulant treatments. 4. Other systemic conditions like diabetes mellitus, high blood pressure, heart diseases, Ulcerative Colitis, Crohn s Diseases and Tuberculosis etc. 5. Pregnant women.

Design outcomes

Primary

MeasureTime frame
Releif in subjective parameters 1. Pain 2. Anal discomfort 3. Size of pile massTimepoint: The patient will be assessed at baseline,then at 1st week,then at 2nd week,then at 3rd week and finally at 4th week at the time of the trial completion.

Secondary

MeasureTime frame
Relief in objective parameters 1.Degree of hemorrhoidal prolapse 2. No. of hemorrhoidal columns involved 3.Relation to dentate line 4. BleedingTimepoint: The patient will be assessed at baseline,then at 1st week,then at 2nd week,then at 3rd week and finally at 4th week at the time of the trial completion.

Countries

India

Contacts

Public ContactDr Bhoomi Soni

Quadra Insitute of Ayurveda and Hospital

Bhoomi629@gmail.com9008637659

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026