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Clinical Trials/ACTRN12615000505505
ACTRN12615000505505
Completed
未知

The Relationship between Sleep Quality and Target Effect-site Propofol Concentration of Target-Controlled Infusion in Adult Female Patients Receiving Transvaginal Oocyte Retrieval

Changhua Christian Hospital, Taiwan (R.O.C.)0 sites200 target enrollmentMay 20, 2015
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ConditionsSleep qualityPropofol required during Transvaginal Oocyte RetrievalAnaesthesiology - AnaestheticsReproductive Health and Childbirth - Fertility including in vitro fertilisation

Overview

Phase
未知
Intervention
Not specified
Conditions
Sleep quality
Sponsor
Changhua Christian Hospital, Taiwan (R.O.C.)
Enrollment
200
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 20, 2015
End Date
TBD
Last Updated
6 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Changhua Christian Hospital, Taiwan (R.O.C.)

Eligibility Criteria

Inclusion Criteria

  • •Female patients assessed as the American Society of Anesthesiologists (ASA) physical status classification system class I and II who are ready for transvaginal oocyte retrieval

Exclusion Criteria

  • •(1\) refusal to provide informed consent,
  • •(2\) allergy to intravenous propofol, fentanyl, or lidocaine,
  • •(3\) hepatic, renal, or neurological dysfunction

Outcomes

Primary Outcomes

Not specified

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