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A clinical trial on Kaattu Vakai Pattai Chooranam in the management of Raththamoolam (Bleeding haemorrhoids)

A prospective open labelled,Non-Randomized,Phase II,Clinical trial of "Kaattu Vakai Pattai Chooranam "in the management of "Raththamoolam"(Bleeding Haemorrhoids)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032371
Enrollment
60
Registered
2021-03-30
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Interventions

Intervention1: Kaattu Vakai Pattai Chooranam: 2g/Twice a day(orally)A/F with ghee for 45 days Control Intervention1: Nil: Nil

Sponsors

Government siddha medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who will be having classical symptoms of bleeding piles (1st degree internal haemorrhoids)i.e. constipation, bleeding per anus,itching in the perianal region. Patients who are all willing to give blood samples at subsequent visit are involved in this study. Patient willing to sign the informed consent starting that he/ she will conscientiously stick to the treatment during 45 days but can opt of the trail of his/her own conscious discretion.

Exclusion criteria

Exclusion criteria: Patients of age below 18 years and above 60 years. Patients having 2nd ,3rd degree internal haemorrhoids. Pregnancy. Fissure in ano. External haemorrhoids. Fistula in ano. Diabetes mellitus. Hypertension. Rectal cancer.

Design outcomes

Primary

MeasureTime frame
Outcome of the treatment is mainly assessed by reduction in clinical symptoms and by comparing the following parameters before and after treatment. Bleeding per rectum. Proctoscopy.Timepoint: 45 days

Secondary

MeasureTime frame
To evaluate Physico Chemical, PhytoChemical,Bio Chemical analysis. To evaluate safety profile for acute and sub-acute toxicity of trial drug Kaattu Vakai Pattai Chooranam To determine about Antimicrobial activities in different Solvents. To evaluate additional effects &Siddha parameters, Envagaithervukal in Raththa Moolam To evaluate the efficacy of Kaattu Vakai Pattai Chooranam on Raththamoolam by the Biostatistical analysis.Timepoint: 45 days

Countries

India

Contacts

Public ContactDrAManoharan

Government siddha medical college and hospital

siddhadrgs21@gmail.com9443358271

Outcome results

None listed

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