A Clinical Trial to Study the Effect of Local Anasthesia Through the palate and through the nose to Assess the blood loss , operating time in Patients Undergoing surgery for Sinus infectio
- Conditions
- Health Condition 1: J329- Chronic sinusitis, unspecified
- Registration Number
- CTRI/2018/08/015178
- Lead Sponsor
- Dr R Premnath
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients Diagnosed with Chronic Rhinosinusitis with or without Polyps not Responding to Medical Management
2.Patients Ready to Give Informed Consent
3.Patients of Either Sex
4.Patients Above 18 Years and Below 60 Years
5.Patients with Hb >10 gm/dl
6.Patients with Normal Bleeding Time, Clotting Time, Prothrombin Time, Activated Partial Thromboplastin Time, International Normalised Ratio (INR)
1.Patient not Ready to Give Informed Consent
2.Patients Below the Age of 18 Years
3.Patients with Active Sinonasal Infection.
4.Patient with Chronic Illness Like Diabetes, Bleeding disorders, Renal failure, Thrombosis, Cirrhosis
5.Patient on Any Anticoagulants
6.Patient not Willing to Participate in the Study
7.Patients having Biopsy Proven Tumors of Nose and Para Nasal Sinuses
8.Patients who are Allergic To Lignocaine
9.Pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method