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N/A Completed N=22 Randomized Single-blind Health Services Research

Improved Patient Recovery After Anesthesia With Hypercapnia Hyperpnoea

Hypercapnia
Source: ClinicalTrials.gov NCT00708526 ↗
Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Oct 2011
Primary outcomePrimary: Recovery From Anesthesia — 53.0; 62.9 minutes — p=>0.05

Summary

The proposed study will measure the time from the end of surgery until the time patients meet the discharge criteria from the postoperative anesthesia care unit and the time from the end of surgery until the patients regained cognitive function after anesthesia.

Outcome Measures

OutcomeResultp-value
PRIMARY
Recovery From Anesthesia
53.0; 62.9 >0.05
SECONDARY
Return of Cognitive Function
10.9; 18.2 0.039 sig

Eligibility Criteria

Inclusion Criteria

  • adults
  • ASA class I-III
  • both genders
  • scheduled to undergo eye surgery at the Moran Hospital.

Exclusion Criteria

  • a history of renal or hepatic disease,
  • chronic alcohol or drug abuse,
  • disabling neuropsychiatric disorder,
  • hypersensitivity or unusual response to other halogenated anesthetics,
  • pulmonary hypertension,
  • increased intracranial pressure,
  • seizure disorder
  • personal/familial history of malignant hyperthermia.
  • currently being treated with known hepatic enzyme-inducing drugs (e.g., phenobarbital, dilantin or isoniazid)
  • or with drugs known to alter anesthetic requirements (e.g., opiates, clonidine, alpha2 agonists, alcohol, anticonvulsants, antidepressants, barbiturates, benzodiazepines or other tranquilizers).
  • intolerance to non-steroidal anti-inflammatories.
  • have received general anesthesia within the previous 7 days,
  • received any investigational drug within the previous 28 days,
  • participated in a previous isoflurane or desflurane study
  • Female subjects can be neither pregnant nor breast feeding.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00708526). 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. Informational only — not medical advice.

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