To assess which mask is comfortable for the patient

Phase 4

Conditions: Health Condition 1: J962- Acute and chronic respiratory failureHealth Condition 2: J810- Acute pulmonary edemaHealth Condition 3: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified

Registration Number: CTRI/2023/11/059792

Lead Sponsor: All India Institute of Medical sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

All patients of either sexes, aged >18 years whether medical or post-surgical who will be fulfilling the criteria of NIV support which include

1.Acute respiratory failure type2

2.Pulmonary edema

3. Weaning in high-risk surgeries

4.Weaning after using mechanical ventilator >7 days

5.Weaning after continuous sedation >72 hrs

6.APACHE II >17.5

Exclusion Criteria

Patients who refused to give consent , hemodynamically unstable, morbidly obese, depressed consciousness, and have improper NIV mask fitting will be excluded from the study.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To determine Comfort of patient assessed by using LIKERTS scaleTimepoint: To determine Comfort of patient assessed by using LIKERTS scale after 4 hours i.e after using both masks for 2 hours each

Secondary Outcome Measures

Name	Time	Method
1, Assessing Blood gas Parameters like PH, PCO2. PO2, HCO3, Na/K <br/ ><br>2, Assesing Physiological parameters Like respiratory rate, Blood pressure, SPO2, Pulse rate <br/ ><br>3, Assesing Ventilator parameters like leakage, fio2 <br/ ><br>4, Complications of NIV mask like facial skin erythema, nasal congestion, nasal or oral dryness, nose/sinus/ear pain, airways dryness <br/ ><br>Timepoint: The hemodynamic parameters such as RR, HR, NIBP/ABP, and SpO2 will be recorded every 30 minutes. <br/ ><br>Ventilatory parameters like fio2 and leakage hrly The ABG sample will be taken at baseline and every 2 hours during the intervention. Complications of NIV mask-like facial skin erythema, nasal congestion, nasal or oral dryness, nose/sinus/ear pain, and airway dryness will be assessed after the intervention. <br/ ><br>