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clinical comparative study of unani drug in chronic rhinosinusitis

A Clinical Study of Waram-e-Tajaweef-e-Anf Muzminâ?? (Chronic Rhinosinusitis) and the Comparative Evaluation of Sharbat-e-Banafsha and Joshandha Gaozaban in its Management

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051601
Enrollment
50
Registered
2023-04-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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: Sharbat-e-Banafsha (oral): Sharbat-e-Banafsha will be given in the dose of 25 ml twice a day orally for 6 weeks Control Intervention1: Joshandha Gaozaban(oral): Joshandha Gaozaban will

Sponsors

State Unani Medical College Prayagraj
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients fulfilling AAO-HNS criteria that is at least two major criteria (Nasal obstruction or blockage, anterior or posterior nasal discharge, Facial pain /congestion, Purulence in a nasal cavity on examination, Anosmia/ Hyposmia) or one major and two minor criteria (Halitosis, earache, dental pain, cough, fatigue) 2 patients had an opacity of X-ray paranasal sinuses (waters view) ranging from +1 (Mucosal thickening) to +3 (complete opaque antrum) grading. 3 Patients of either sex. 4 Patients in the age group of 18 to 60 years. 5 Patients with involvement of any sinus. 6 Those who give written consent.

Exclusion criteria

Exclusion criteria: 1 Child below 18 years of age. 2 Patients above 60 years of age. 3 Pregnant & lactating mothers. 4 Patients who fail to give consent. 5 Patients who fail to follow up. 6 Mentally retarded persons. 7 Patients with Malignancy of the nose or paranasal sinuses. 8 Patients have a history of any surgery of the nose or paranasal sinuses. 9 Patients have a history of any foreign body in their nose. 3Patient have a history of trauma to the nose or sinus areas. 10 Patients suffering from any congenital or acquired structural abnormality of the nasal cavity. 11 Any medical condition where the physician feels that participation in the study could be detrimental to patientsÂ? wellbeing. 12 Patients of pulmonary Kochs or patients having history of epistaxis

Design outcomes

Primary

MeasureTime frame
1 reduction in AAO-HNS criteria 2 reduction in X-ray paranasal sinuses (waters view) ranging from +1 (Mucosal thickening) to +3 (complete opaque antrum) grading.Timepoint: 0 and 6 week

Secondary

MeasureTime frame
improvement in clinical featuresTimepoint: 0 and 6 week

Countries

India

Contacts

Public ContactDr Usamah Ahmad

state Unani Medical College

asifhussainusmani@gmail.com7905831926

Outcome results

None listed

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