Rocuronium Dose Finding Study After Single-shot or Steady-state Propofol Anesthesia
NCT02054468 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82
Last updated 2014-05-08
Summary
This study is designed to determine the effective-doses ED-50 and ED-95 (the doses required for a 50% and 95% twitch inhibition, respectively) of the non-depolarizing muscle relaxant rocuronium after single-shot or steady-state propofol anesthesia in a clinical setting.
Conditions
- Neuromuscular Blockade
- Anesthesia
Interventions
- DRUG
-
Single-Shot Propofol
Single-shot propofol induction dose (1.5-2.5mg/kg body mass)
- DRUG
-
30min infusion Propofol
30min of propofol infusion (4-6mg/kg/h)
- DRUG
-
Remifentanil infusion
Remifentanil infusion (0.1-0.2µg/kg/min)
- DRUG
-
Rocuronium (0.07mg/kg/body mass)
Rocuronium (0.07mg/kg/body mass)
- DRUG
-
Rocuronium (0.1mg/kg/body mass)
Rocuronium (0.1mg/kg/body mass)
- DRUG
-
Rocuronium (0.15mg/kg/body mass)
Rocuronium (0.15mg/kg/body mass)
- DRUG
-
Rocuronium (0.2mg/kg/body mass)
Rocuronium (0.2mg/kg/body mass)
- DRUG
-
Rocuronium (0.3mg/kg/body mass)
Rocuronium (0.3mg/kg/body mass)
- DRUG
-
Rocuronium (0.45mg/kg/body mass)
Rocuronium (0.45mg/kg/body mass)
Sponsors & Collaborators
-
Technical University of Munich
lead OTHER
Principal Investigators
-
Manfred Blobner, M.D. · Klinik für Anaesthesiologie, Klinikum rechts der Isar der Technischen Universität München, Ismaninger Str. 22, 81675 München, Germany
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-03-31
- Primary Completion
- 2014-02-28
- Completion
- 2014-02-28
Countries
- Germany
Study Locations
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