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Personalized Healing for Hemorrhoids: Insights from Homeopathic Treatment

Enhancing Quality of Life: A Prospective, Interventional Study on Individualized Homoeopathic treatment for hemorrhoids using the Synthesis Repertory - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065829
Enrollment
30
Registered
2024-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: K642- Third degree hemorrhoids

Interventions

Intervention1: Homoeopathic medicine after individualization obtained through repertorization by using Synthesis repertory: Homoeopathic medicine obtained after repertorisation from Synthesis Repertor

Sponsors

Dr Rashmi more
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Patients with Grade I, II, III hemorrhoids ii. Diagnostic criteria are mainly based on the clinical presentation

Exclusion criteria

Exclusion criteria: i.Patients with Grade IV hemorrhoids ii.Pregnant women. iii.Patients suffering from other diseases affecting anorectal region like fissure in ano, fistula in ano, malignancy, anorectal abscess, Crohn’s disease, ulcerative colitis, rectal polyp, and other diseases having rectal complaints as secondary phenomena.

Design outcomes

Primary

MeasureTime frame
Assessment of impact of homoeopathic treatment for haemorrhoids on quality of life.Timepoint: Assessment of impact of homoeopathic treatment for haemorrhoids on quality of life. Duration of first follow up will be 7 days to 15 days after the prescription, then depending on the case assessment medicine will be repeated and potency will be changed as per the requirement of the case. Further follow ups will be taken every fortnightly; every case will be followed up for 3 months.

Secondary

MeasureTime frame
Assessment the effects of homoeopathic treatment on symptoms like pain, bleeding, discharge, & itching in terms of frequency, intensity & duration of study.Timepoint: Symptoms like pain, bleeding, discharge, & itching in terms of frequency, intensity & duration of study will be assessed during f/u. After the first follow up which will be after 7 days to 15 days then depending on the case assessment administered medicine in potency of 30, 200, 1M as per the requirement of the patient & will be repeated & the potency will be changed as per the requirement of the case. Further f/u will be taken every fortnightly every case will be followed up for 3 months

Countries

India

Contacts

Public ContactDr Rashmi More

Assistant Professor

rashmi.more@bharatividyapeeth.edu9503230236

Outcome results

None listed

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