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N/A N=4,000

Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesia With Sevoflurane

Anesthesia, General

Enrolled (actual)
4,000
Serious AEs
0.0%
Results posted
Jan 2012
Primary outcome: Primary: Anesthesiologist Satisfaction With the Anesthesia Recorded at the End of the Operation Using a Numeric Analog Scale (NAS) — 8.85 units on a scale

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Abbott
Primary completion
Nov 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Anesthesiologist Satisfaction With the Anesthesia Recorded at the End of the Operation Using a Numeric Analog Scale (NAS)
8.85
PRIMARY
Patient Satisfaction With the Anesthesia Recorded at the End of the Operation Using a Numeric Analog Scale (NAS)
8.88
SECONDARY
Time to Loss of Consciousness of Patients Administered Anesthesia
1.65
SECONDARY
Time to Intubation of Patients
4.06
SECONDARY
Time to Eye Opening of Patients
14.02
SECONDARY
Time to Extubation of Patients
16.33

Summary

This registry is primarily aiming to demonstrate the correlation between good practices of anesthesiologists and patient related outcomes including decreased overall anesthesia cost. The investigators would also like to demonstrate how the training background, and experience in inhalational anesthesia of the anesthesiologist influence their daily practice. At the end of the registry, the investigators would be able to demonstrate the influence of different practice pattern on patient related outcomes between the sites at which anesthesiologists follow modern anesthesiology practice based on their training/experience background and at which anesthesiologists do not follow same type of practice due to lack of their inhalational anesthesia training/experience.

Eligibility Criteria

Inclusion Criteria

  • ASA (American Society of Anesthesiologists) physical status (a requirement of the patient's physical status): I to III
  • Age from 18 to 70 years
  • Surgery requiring general anesthesia with endotracheal intubation or laryngeal mask airway.

Exclusion Criteria

  • History of significant cardiovascular, pulmonary, renal, hepatic or central nervous system disease or muscle disease.
  • Hypersensitivity or unusual response to any halogenated anesthetics.
  • Personal or familial history of malignant hyperthermia.
  • Female patients either pregnant or breast feeding.
  • General anesthesia is administered with total intravenous anesthesia (TIVA) of propofol.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01199471). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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