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van CCT (UK)

van CCT (UK)

Ademhalingsstudie naar de interactie tussen remifentanil en propofol in gezonde vrijwilligers.

- candidate number8731
- NTR NumberNTR2637
- ISRCTNISRCTN wordt niet meer aangevraagd.
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR3-dec-2010
- Secondary IDsP10.017 / NL31225.058.10 ; METC LUMC / CCMO
- Public TitleAdemhalingsstudie naar de interactie tussen remifentanil en propofol in gezonde vrijwilligers.
- Scientific TitleModeling the respiratory effects of subanesthetic doses of PROPofol under closed-loop or non-steady-state conditions without and with a remifentanil background infusion in healthy volunteers.
- hypothesisA mathematically correct PK-PD model will be developed that describes the depressant effect of propofol on breathing with and without a background of remifentanil.
- Healt Condition(s) or Problem(s) studiedRespiration, Healthy subjects, Remifentanil , PK-PD, Propofol
- Inclusion criteria1. Healthy volunteers of either sex;
2. Age 18-45 years.
- Exclusion criteria1. BMI > 35;
2. Presence of any medical disease;
3. History of drug or alcohol abuse;
4. Allergy to study medications;
5. Mallampati 3 or greater;
6. For females: Use of contraceptives required.
- mec approval receivedyes
- multicenter trialno
- randomisedyes
- masking/blindingSingle
- controlNot applicable
- groupCrossover
- Type2 or more arms, randomized
- Studytypeobservational
- planned startdate 18-nov-2010
- planned closingdate1-jun-2011
- Target number of participants24
- Interventions24 volunteers will participate in two experimental runs lasting about 1 hr with a 2 hr washout period in between. During each experimental run a 30 minutes infusion of propofol (first run) or propofol + a steady state background of remifentanil (second run) will be performed. The propofol infusion will be divided in three steps (Target Plasma Concentration of 0.7, 1.4 or 2.1 mcg/ml) that will be administrated in a randomized order. All subjects will receive all steps in propofol. The remifentanil infusion will be a steady state infusion of 0.8 ng/ml or 1.6 ng/ml. This will be randomized and each volunteer will receive one of these background infusion levels. After the 30 minutes infusion an additional 30 minutes of data sampling will be performed for the washout period.
We will perform bloodsampling regularly via an arterial line. Furthermore we will measure ventilation and EEG via BISmonitoring.
- Primary outcome1. Ventilation (l/min);
2. EEG monitoring via BIS;
3. Bloodsampling for propofol concentrations.
- Secondary outcome1. Cardiac output;
2. Heartrate;
3. Saturation.
- TimepointsFirst run:
30 minutes infusion of 3 three steps of 10 minutes in different Plasma Target Concentrations (0.7, 1.4, 2,1 ng/ml). Heartrate, saturation, EEG/BIS will be measured continously. Bloodsampling will be performed at baseline, 2 minutes after a step change, 5 minutes after a stepchange and just prior to a stepchange (app. at 10 minutes). Bloodsampling will be continued at intervals of 10 minutes untill 30 minutes after the end of the infusion.
After a 2 hr break we will perform the second run. The second run will be identical to the first, except for a steady state background infusion of remifentanil at 0.8 or 1.6 ng/ml.
- Trial web siteN/A
- statusopen: patient inclusion
- Sponsor/Initiator Leiden University Medical Center (LUMC)
- Funding
(Source(s) of Monetary or Material Support)
Leiden University Medical Center (LUMC)
- PublicationsN/A
- Brief summaryA study aimed at PK-PD modelling of the respiratory effects of propofol in healthy volunteers in different plasma target concentrations, with and without a background infusion of remifentanil.
- Main changes (audit trail)
- RECORD3-dec-2010 - 15-dec-2010

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