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Study to evaluate efficiency of pressure support ventilation in prolongation of safe apnea time in obese adults scheduled for elective surgery

Comparative evaluation of preoxygenation using pressure support ventilation v/s conventional method in obese adults scheduled for elective surgery - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066045
Enrollment
36
Registered
2024-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: Preoxygenation with 12cmH2O pressure support in intervention group: Standardized anaesthesia protocol will be followed. Peripheral intravenous line will be secured with appropriate size

Sponsors

Pt BDSharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients with age 20 to 60yr with BMI 25to 40, American society of anesthesiology ASA grade I and II with mallampati score I and II with thyromental distance more than 6cm

Exclusion criteria

Exclusion criteria: Patient refusal to participation Difficult mask ventilation including bearded,edentulous COPD, Bronchial Asthma,URTI Pregnancy Congenital heart disease Coagulation and bleeding abnormalities Breath holding less than 20 sec Risk of aspiration

Design outcomes

Primary

MeasureTime frame
Number of patients achieving EtO2 90% in 3minTimepoint: At 3min

Secondary

MeasureTime frame
Discomfort during preoxygenation if anyTimepoint: To be asked in postoperative room;Effect on Safe Apnea timeTimepoint: Time after 90sec of rocuronium administration to SpO2 fall to 93%;Gastric insufflation if anyTimepoint: During preoxygenation;Preoxygenation timeTimepoint: Time taken to achieve EtO2 90%

Countries

India

Contacts

Public ContactDr Priti

Pandit B.D.Sharma PGIMS Rohtak

susheelataxak@gmail.com9896067416

Outcome results

None listed

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