Skip to content

A Study Comparing Two Ayurvedic Nasal Treatments for Frontal Sinusitis Headache

A Comparative Clinical study to Evaluate the Efficacy of Ikshu Ardraka Avapeeda Nasya with Vacha Pippali Avapeeda Nasya in Suryavarta with reference to Frontal sinusitis - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/113185
Enrollment
40
Registered
2026-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: J348- Other specified disorders of noseand nasal sinuses

Interventions

None listed

Sponsors

Dr Shailashree
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects presenting with classical symptoms of Suryavarta and frontal sinusitis, including Shirashoola dinavrudha vivardhate, along with any one or more of the following symptoms: Pain in the forehead . Pain around or behind the eyes. Pain in the temporal region. Pulsating type of pain. Tenderness over the frontal sinus area 2 Subjects between 16 and 60 years of age. 3 Subjects with a disease chronicity of less than 3 years.

Exclusion criteria

Exclusion criteria: 1 Pregnant and lactating women. 2 Subjects with complication of sinusitis. 3 Subjects who are contraindicated for Nasya. 4 Patient with other systemic disorders.

Design outcomes

Primary

MeasureTime frame
To evaluate the therapeutic efficacy of Ikshu- Ardraka Avapeeda Nasya in the management of Suryavarta (Frontal sinusitis).Timepoint: 0,7,14,28,52 day

Secondary

MeasureTime frame
To compare the clinical outcomes of Ikshu-Ardraka Avapeeda Nasya and Vacha-Pippali Avapeeda Nasya in the management of Suryavarta(Frontal sinusitis)Timepoint: 0,7,14,28,52 day

Countries

India

Contacts

Public ContactDr Satheesha Shankara

Alvas Ayurveda medical college and hospital moodbidre

drsatish88@gmail.com9482167168

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026