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A clinical trial to study the efficacy of Siddha formulation in patients with Sinusitis

An open labeled clinical trial on peenisam (Sinusitis) - CTP-APNC

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/08/003930
Enrollment
30
Registered
2013-08-29
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: null- Sinusitis

Interventions

Intervention1: Capsule APNC. A combination of Seenthil chooranam (400mg) with Aya Poonaga Chenduram (100mg]: 1 capsule B.I.D with water. mode of administration: oral. duration: 42 days Control Interve

Sponsors

Central Council for Research in Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients suffering with the following Complaints Rhinorrhea, Redness & lacrimation of the eyes, Nasal congestion, Nasal Speech Itching & blockage of ears Difficulty in breathing Head ache Post Nasal drip Giddiness Dull ache in mid face or Deep into Eyes Sneezing Chronic hyperplastic Sinusitis (Nasal polyp) Deviated Nasal Septum (DNS) and patient conformed with X Ray PNS - Sinusitis - Positive

Exclusion criteria

Exclusion criteria: The following conditions are excluded 1. Bacteremia /Glaucoma/Trachoma 2. Meningitis /Aneurysms of arteries of brain 3. Acute Pyrexia/SOL 4. Habitual snuffer 5. Epistaxis / Saddle nose / Syphilitic chancre 6. DM/Thyroid/HT/Trigeminal Neuralgia/Dental caries 7. Hansenâ??s Disease 8. Bronchial Asthma

Design outcomes

Primary

MeasureTime frame
Integrated Medicine Outcome Scale (IMOS) Reduction of symptoms and decrease in the time intervals of episodesTimepoint: 42 days

Secondary

MeasureTime frame
Assessment of the drug safety of APNC in PeenisamTimepoint: 42 Days

Countries

India

Contacts

Public ContactDr M Kannan

Siddha Central Research Institute

siddhikanna@gmail.com04426214809

Outcome results

None listed

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