Herzzentrum Leipzig GmbH
Leipzig, 04289, Germany
NCT Number: NCT01937767
This phase II study in patients undergoing elective cardiac surgery will evaluate the efficacy, safety, and pharmacokinetics of remimazolam, compared with propofol and sevoflurane, during the induction and maintenance of general anesthesia.
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All sexes
Interventional
Phase 2
Leipzig, 04289, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: ByFavo, Aptimyda, CNS7056
Other names: Propofol-®Lipuro 10 mg/ml
Other names: Sevofluran Baxter
Other names: Ultiva (remifentanil hydrochloride) for Injection
Other names: Fentanyl-Janssen
Other names: Esmeron 10mg/ml solution for injection
Time frame: Between the start of study medication and the end of the surgical procedure (up to approx 12 hours)
Successful anesthesia was defined as no use of rescue sedative medication between start of the study medication and end of the surgical procedure completion of last skin suture.
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Industry
A Randomized, Single-blind Phase II Study Evaluating the Efficacy, Safety and Pharmacokinetics of Remimazolam in General Anesthesia in Adult Patients Undergoing Cardiac Surgery, Including Follow-up Sedation in the PACU/ICU
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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