CTRI/2024/04/064979
Not Yet Recruiting
N/A
Comparative Evaluation Of Therapeutic Efficacy And Safety Of Intranasal Fluticasone Furoate And Fluticasone Propionate In Patients Of Chronic Rhinosinusitis: A Randomized, Open Label, Parallel Group Study - nil
Govt Doon Medical college0 sites0 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Health Condition 1: J329- Chronic sinusitis, unspecifiedHealth Condition 2: J329- Chronic sinusitis, unspecified
- Sponsor
- Govt Doon Medical college
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Newly diagnosed cases of chronic rhinosinusitis in age group of 18\-60 years .
- •2\. Patients giving valid informed consent.
Exclusion Criteria
- •1\. Cases having active upper air way infection, malignant / benign mass of nose and PNS and post\-operative cases of functional endoscopic sinus surgery.
- •2\. Patient having symptomatic gross Deviated Nasal Septum(DNS),Septal perforation and/or Nasal polyps, severe epistaxis, purulent nasal infection
- •3\. Patients refusing to participate in the study.
- •4\. Dependence on prolonged corticosteroid therapy for comorbid conditions, such as asthma and chronic obstructive pulmonary disease
- •5\. History of allergy to fluticasone propionate or fluticasone furoate or other topical steroids.
- •6\. History of clinically significant cardiac, renal, psychiatric, hepatic and endocrine disease.
- •7\. Pregnant or breastfeeding females.
- •8\. Known immunodeficiency state.
- •9\. Patients of Fungal Rhinosinusitis.
Outcomes
Primary Outcomes
Not specified
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