UnknownN/Aketamine

Respiratory Depression During an Analgosedation Combining Remifentanil and Ketamine in TCI for Oocyte Retrieval

Sponsored by Erasme University Hospital

NCT ID
NCT03458143
Target Enrollment
20 participants
Start Date
2018-02-12
Est. Completion
2018-03-31

About This Study

This study evaluates the effect of the addition of ketamine to a conscious sedation protocol including remifentanil during oocyte retrieval. The investigators will have 2 groups with different target effect site concentrations, namely 150 ng/ml and 200 ng/ml.

Conditions Studied

Oocyte RetrievalSedation, ConsciousVentilatory Depression

Interventions

  • Ketamine 150 ng/ml
  • Remifentanil
  • Oocyte retrieval
  • Ketamine 200 ng/ml

Eligibility

Sex:FEMALE
Age:18 Years - N/A
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* patients having an oocyte retrieval

Exclusion Criteria:

* BMI \> 30
* endometriosis
* contraindications to ketamine

Study Locations (1)

Erasme University Hospital
Brussels, Belgium

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source