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A clinical study on Waram-e-tajaweef anf muzmin (chronic rhinosinusitis) and comparative evaluation of qurs e musakkin and mufeed joshanada in its management

A Clinical Study on Warm-e Tajaweef-e-Anf-Muzmin (Chronic Rhinosinusitis) and Comparative Evaluation of Unani Formulations in its Management:A Randomized,single blind parallel Group comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036532
Enrollment
100
Registered
2021-09-15
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: J329- Chronic sinusitis, unspecified

Interventions

None listed

Sponsors

Department of moalejat Ajmal khan tibbiya college and hospital Aligarh muslim university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients fulfilling AAO-HNS criteria that is atleast two major criteria (Nasal obstruction or blockage ,anterior or posterior nasal discharge ,Facial pain /congestion , Purulence in nasal cavity on examination ,Anosmia/ Hyposmia ) or one major and two minor criteria (Halitosis , earache, dental pain , cough , fatigue) patients having opacity of Xray paranasal sinuses ( waterâ??s view )ranging from +1 (Mucosal thickening )to +3 (complete opaque antrum) grading. Patients of either sexes. Patients in the age group of 15 to 50 years. Patients with involvement of any sinus. Those who give written consent.

Exclusion criteria

Exclusion criteria: 1.Children below 15 years of age. 2.Patients above 50 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 having history of any surgery of nose or paranasal sinuses. 9.Patients having history of any foreign body in their nose. 10.Patient having history of trauma to nose or sinus areas. 11.Patients suffering from any congenital or acquired structural abnormality of the nasal cavity. 12.Any medical condition where physician feels that participation in the study could be detrimental to patientâ??s well being. 13.Patients of pulmonary kochâ??s or patient having history of epistaxis.

Design outcomes

Primary

MeasureTime frame
Improvement in clinical featuresTimepoint: Weekly for 6 weeks

Secondary

MeasureTime frame
Changes in the X-ray PNS waters view with the help of an arbitrary scaleTimepoint: At start of the intervention and at the end of the 6 week

Countries

India

Contacts

Public ContactFoziya KHANAM

Department of moalejat Ajmal khan tibbiya college and hospital AMU

misbahuddin.dr1980@gmail.com9837030145

Outcome results

None listed

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