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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 infection

Effect of Greater Palatine Block and Intranasal Block in Surgical Outcomes of Functional Endoscopic Sinus Surgery - A Randomised Controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015178
Enrollment
60
Registered
2018-08-03
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

Intervention1: Functional Endoscopic Sinus Surgery using A Conventional Intranasal Block or Greater Palatine Canal Block: Functional Endoscopic Sinus Surgery is done for Patients with Chronic Rhinosin

Sponsors

Dr R Premnath
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 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)

Exclusion criteria

Exclusion criteria: 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

Design outcomes

Primary

MeasureTime frame
Intra Operative assessment of Blood Loss, Quality of Surgical Field Using Boezaarts Scale and Total Operating TimeTimepoint: 1.15 minutes 2.30 minutes 3.45 minutes after start of surgery 4.End of aurgery

Secondary

MeasureTime frame
Overall Surgical OutcomeTimepoint: At the End of Surgery

Countries

India

Contacts

Public ContactDr D AnandKarthikeyan

SRM Medical College and Research Centre

entpurush@gmail.com9840723243

Outcome results

None listed

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