Improved Patient Recovery After Anesthesia With Hypercapnia Hyperpnoea (NCT00708526) | Clinical Trial Compass
CompletedNot Applicable
Improved Patient Recovery After Anesthesia With Hypercapnia Hyperpnoea
United States22 participantsStarted 2008-03
Plain-language 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.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.