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A Clinical Trial Based On Exciting and Maintaining Causes In Management Of Tonsillitis By Homoeopathy

Clinical Study On The Utility Of Individualised Homoeopathic Medicines Based On Exciting And Fundamental Causes In Management Of Tonsillitis - A Prospective Open Arm Interventional Study - MOTH

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066590
Enrollment
30
Registered
2024-05-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: J350- Chronic tonsillitis and adenoiditis

Interventions

Intervention1: Individualized Homoeopathic medicine: Intervention is planned as administering individualized homoeopathic medicine to a group of 30 patients suffering from Tonsillitis after detailed c

Sponsors

Himalaya Sahu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient with age group 05 to 50 of both sexes having tonsillitis 2.Presenting with clinical signs and symptoms of chronic tonsillitis – presence of any symptoms: hyperaemia of anterior and posterior palatine arches, enlarged submandibular lymph nodes, halitosis, chronic sore throat, foreign body sensation or a history of expelling foul-tasting and foul smelling cheesy lumps. 3.Patient who are newly diagnosed with clinical acute tonsillitis. 4.Patients who can give consent informed and comply with study procedure

Exclusion criteria

Exclusion criteria: 1. Patient with complications like Quinsy, Septic focus, Septicemia, Laryngeal oedema, Pharyngeal or Retropharyngeal abscess. 2. Diagnosed cases of Adenoids, Obstructive sleep apnea and Acute rheumatic fever. 3. Patient who require medical emergency intervention and systemic disease with intervention. 4. Presence of neurological or psychiatric diseases affecting quality of life. 5. Cases already undergoing homeopathic treatment for any chronic diseases. 6. Pregnant, puerperial and lactating women.

Design outcomes

Primary

MeasureTime frame
Friedman Grading Scale For TonsilsTimepoint: Improvement in the Friedman Grading Scale For Tonsils at day 1 and again after 15 day upto 6 months

Secondary

MeasureTime frame
Visual analogue scale based on severity scoreTimepoint: Day 0,1,2,3,4,5,6 and7

Countries

India

Contacts

Public ContactDr Archna Kumari

State National Homoeopathic Medical College and Hospital

archna505@gmail.com9450522295

Outcome results

None listed

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