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To evaluate the peripheral oxygen saturation on extubation in lateral versus supine position in adult patients undergoing oral surgery.

Evaluation of peripheral oxygen saturation on extubation in lateral versus supine position in adult patients undergoing oral surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053428
Enrollment
80
Registered
2023-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Extubation.: Peripheral oxygen saturation levels on extubation in supine position in adult patients undergoing oral surgery. Control Intervention1: Extubation.: Peripheral oxygen satura

Sponsors

Dr. Sarvjeet Kaur
Lead Sponsor
Dr Haramritpal Kaur
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients belonging to American Society of Anesthesiologist Grade I and II. 2. Patients aged from 18-60 years old. 3. Patients schedule for elective oral surgeries.

Exclusion criteria

Exclusion criteria: 1. Patient with history of current cough, recent upper respiratory tract infections. 2. Patient with history of chronic cough, chronic upper airway disease, chronic obstructive lung diseases, asthma, allergic rhinitis. 3. Patient with obstructive sleep apnea syndrome, severe snoring. 4. Patient with BMI >35kg/m2.

Design outcomes

Primary

MeasureTime frame
1. To evaluate the peripheral oxygen saturation level while extubation in supine position. 2. To evaluate the peripheral oxygen saturation level while extubation in lateral position. 3. To compare the peripheral oxygen saturation level while extubation in supine position versus lateral position.Timepoint: Outcome will be assessed at the end of study that is 18 months.

Secondary

MeasureTime frame
1. To evaluate airway related complications such as coughing, laryngoapasm, non purposeful movements, breath holding.Timepoint: Outcome will be assessed at the end of study that is 18 months.

Countries

India

Contacts

Public ContactGagandeep Kaur

Guru Gobind Singh Medical College and Hospital

drsarvjeetk@gmail.com9915680508

Outcome results

None listed

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