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Kundalathy Legiyam for the treatment of Maxillary Sinusitis

Clinical Evaluation of Sddha Herbal Formulation Kundalathy Legiyam for the Treatment of Pitha Thalainokkadu(Maxillary Sinusitis)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022740
Enrollment
30
Registered
2020-01-13
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: J320- Chronic maxillary sinusitis

Interventions

Intervention1: Kundalathy Legiyam: Dose:4 gram/bd Adjuvent:Milk Duration :48 days Control Intervention1: NIL: NIL

Sponsors

National Intitute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Maxillary sinusitis associated with or without other sinusitis Nasal congestion,nasal discharge,facial pain or pressure associated referred pain to the ears and teeth, sneezing, headache, cough, fever, fatigue, nausea, hyposmia, anosmia, halitosis Patient having any four of the above mentioned symptoms Patient who are willing to undergo haematological,radiological and otherlaboratory investigations Patient who are willing to sign the informed consent stating that he/she will consciously stick to the treatment during 48 days

Exclusion criteria

Exclusion criteria: Pregnant women and lactating mother Diabetes mellitus Hypertension Cardiac disease Any other serious systemic illness

Design outcomes

Primary

MeasureTime frame
outcome is mainly assessed by clinical symptoms, laboratory and radiological investigationsTimepoint: Fourty Nineth Day

Secondary

MeasureTime frame
The siddha principles like envagai thervu, neerkkuri, neikkuri,udal thathukkal,uyir thathukkal will be studied. The co factors related to this disease such as age, sex, family history, socio economic status, occupational history,dietary habits,personal history related to this disease will be studied. The physico chemical and phytochemical analysis of the study drug will be evaluated. changes in other investigations like TC,DC,ESR,AEC etc.Timepoint: forty five days

Countries

India

Contacts

Public ContactDr Saranya S

National Institute of Siddha,Tambaram Sanatorium.

drlakshmiramaswamy@gmail.com9025575185

Outcome results

None listed

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