To differentiate Tidal volume in two different head position during mask ventillation.
Not Applicable
- Conditions
- Health Condition 1: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified
- Registration Number
- CTRI/2023/09/057948
- Lead Sponsor
- Dr Hari Govindh A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA I and II patients of either sex.
2. Patients aged between 18 to 70 years
3. Patients undergoing general anesthesia with endotracheal intubation.
Exclusion Criteria
1. ASA 3 and ASA 4 patients
2. Patients having allergies to drugs,
3. History of neck pain, giddiness on neck head rotation,
4. History of cervical spine pathology, and patients with co-morbidities (cardiacdiseases,onthyroid medications)
5. Any trauma to the cervical spine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure the tidal volume of the patients in conventional and head rotated position during mask ventillation.Timepoint: To study the duration at 15,30,45,60,75,90,105,120,135,150,160,170 seconds in conventional and head rotated position.
- Secondary Outcome Measures
Name Time Method We will be measuring the expiratory tidal volume, end tidal carbon dioxide & saturation with the conventional approach of bag mask ventilation for the initial 3 minutes at 15 second intervals. The same parameters will be measured for the test group (Group B – with head rotation) at 15 second intervals for 3 minutesTimepoint: To study the duration at 15,30,45,60,75,90,105,120,135,150,160,170 seconds in conventional & head rotated position.