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The Efficacy of Isocapnic Hyperpnoea to Accelerate Recovery After General Anesthesia With Sevoflurane

The Efficacy of Isocapnic Hyperpnoea to Accelerate Recovery After General Anesthesia With Sevoflurane.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00242671
Enrollment
Unknown
Registered
2005-10-20
Start date
2005-10-31
Completion date
2008-12-31
Last updated
2010-08-05

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

Conditions

Anesthesia

Keywords

general anesthesia, hyperventilation, carbon dioxide, isocapnic hyperponea

Brief summary

The twilight phase between being asleep and awake during recovery from anesthesia is a precarious time fraught with risks to the post-operative patient. Hyperventilation accelerates the elimination of inhaled anesthetics but reduces their CO2 blood concentrations which delays their resumption of spontaneous breathing. We previously showed that our method of hyperventilation without affecting the CO2 concentration--which we call IH--accelerates the rate of emergence from anesthesia with isoflurane. In this study we will study the effect of IH on the rate of emergence from Sevoflurane anesthesia.

Interventions

PROCEDUREIsocapnic Hyperponea

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Elective gynecological procedure 2. ASA I-III 3. Age 18-80 years 4. Signed informed consent

Exclusion criteria

1. ASA IV 2. Patients with contra-indications to Sevoflurane anesthesia or other anesthetics included in the protocol 3. Active smoking, asthma or other history of hyper-reactive airway disease 4. History of chronic obstructive lung disease limiting exercise 5. History of angina, previous myocardial infarction, valvular heart disease, or heart surgery 6. Presence of heart murmurs or neck bruits 7. ECT abnormalities including atrial fibrillation, prolonged P-R interval, prolonged Q-T interval, presence of Q waves in inferior, anterior or lateral leads, criteria for left ventricular hypertrophy, T-wave abnormalities, 8. History of difficult airway access 9. Pulmonary hypertension and/or right ventricle dysfunction 10. History of bulous emphysema, and/or spontaneous pneumothorax 11. History of alcohol or drugs abuse 12. Known history of psychiatric illness and/or medications 13. Patients that required postoperative mechanical ventilation for any reason

Design outcomes

Primary

MeasureTime frame
Time to recovery from anesthesia as indicated by time to extubation and rate of change of BIS score

Secondary

MeasureTime frame
Quality of recovery in the recovery room as indicated by the level of consciousness, incidence of nausea, vomiting, shivering and other phenomena occuring during recovery

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026