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A clinical trial to study the effects of herbal medicine in patients with Piles

An Open-Label Pilot Study of Anocurex Kit to Assess its Safety and Efficacy in the Symptomatic Treatment of Hemorrhoids - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105768
Enrollment
24
Registered
2026-03-10
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: I879- Disorder of vein, unspecified

Interventions

None listed

Sponsors

Medi Hero Biotech LLP
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinical diagnosis of haemorrhoids more than 3 months. Participants having symptomatic haemorrhoids Goligher Classification Grade I-II. No need to emergency operation according to physical examination. Sodergren Score less than Capable of and freely willing to provide written informed consent prior to participating in the study.

Exclusion criteria

Exclusion criteria: Inflammatory and infectious disease of the digestive tract (like Inflammatory Bowel Diseases). Acute hemorrhoids or complicated hemorrhoids with bleeding requiring admission, such as strangulated internal hemorrhoids, thrombosed internal or external hemorrhoids. Previous hemorrhoidectomy. Moderate to severe hypertension, cardiovascular diseases, renal failure, cirrhosis, colorectal cancer, anal fissure or fistula. Pregnant woman, lactating woman, and woman of childbearing potential who is planning a pregnancy or is unwilling to use appropriate methods of contraception during the study. Participation in an interventional clinical study or administration of any investigational agents in the previous 30 days.

Design outcomes

Primary

MeasureTime frame
Goligher Classification Grade, Pain, Bleeding conditions, Sodergren Score. Vaizey Score.Timepoint: Day 0, 4 weeks

Secondary

MeasureTime frame
Laboratory safety parameters (FBS, CBC, LFT and kidney function tests). Occurrence of adverse events.Timepoint: 4 WEEKS

Countries

India

Contacts

Public ContactMrs Supriti Choudhury

J. B. Roy State Ayurvedic Medical College and Hospital

srikantapandit@gmail.com09831723650

Outcome results

None listed

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