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Effect of Jadwar in People with Chronic Sinusitis

A Controlled Clinical Study to Evaluate the Safety and Efficacy of Jadwar (Delphinium denudatum) in the Management of Chronic Sinusitis - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105629
Enrollment
60
Registered
2026-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: J329- Chronic sinusitis, unspecified

Interventions

Intervention1: jadwar (Delphinium denudatum): The intervention group will receive Jadwar (Delphinium denudatum) in capsule form at a dose of 500 mg, administered orally twice daily with lukewarm water

Sponsors

Jamia Hamdard University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18 and 60 years of either gender. Clinically diagnosed cases of chronic sinusitis confirmed by nasal endoscopy and/or radiological imaging. Patients experiencing symptoms such as nasal congestion, facial pain or pressure, headache, or post-nasal drip persisting for at least 4 weeks. Patients who are willing to provide written informed consent and comply with the study protocol and follow-up schedule.

Exclusion criteria

Exclusion criteria: Pregnant and lactating women. Patients with a history of recent nasal or sinus surgery. Patients suffering from any major systemic disorder. Patients with immunocompromised conditions such as HIV or tuberculosis. Patients who have used corticosteroids, antibiotics, or other treatments for sinusitis within the past four weeks. Patients with nasal polyps or significant sinonasal structural abnormalities (e.g., markedly deviated nasal septum).

Design outcomes

Primary

MeasureTime frame
Change in total SNOT-22 (Sino-Nasal Outcome Test-22) score in patients with chronic sinusitis treated with Jadwar.Timepoint: Baseline (Day 0) and Day 30

Secondary

MeasureTime frame
Change in quality of life assessed by SF-12 questionnaire.Timepoint: Baseline (Day 0) and Day 30

Countries

India

Contacts

Public ContactDr Shoaib Khan

Jamia Hamdard

dranzaralam@jamiahamdard.ac.in9916164662

Outcome results

None listed

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