NCT Number: NCT02442232
Hemodynamic Changes After Anesthesia With Propofol: Study of Biomarkers
The purpose of this study is to evaluate biomarkers affecting the hemodynamic responses to propofol. Particularly, the investigators will assess the effects of polymorphisms in NOS3 and PRKCA genes on hemodynamic responses to propofol and the effects of these polymorphisms on biomarkers related to nitric oxide after propofol anesthesia. In addition, the investigators will evaluate the effects of propofol anesthesia on biomarkers related to nitric oxide in hypertensive patients chronically treated with angiotensin-converting enzyme inhibitors.
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Conditions
Age range
40 year–80 year
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- ASA I or II
- BMI lower 30 kg/m2
Exclusion criteria
- Severe hypertension
- Previous stroke
- Previous infarction
- Uncontrolled respiratory, renal, hepatic and hematological diseases.
Treatment and study plan
Primary outcomes
-
Systolic blood pressure
Time frame: 10 minutes
-
Diastolic blood pressure
Time frame: 10 minutes
-
Mean blood pressure
Time frame: 10 minutes
-
Heart rate
Time frame: 10 minutes
-
Plasma nitrite levels
Time frame: 10 minutes
-
Plasma nitrate levels
Time frame: 10 minutes
Sponsors and collaborators
Lead sponsor
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Other Gov
Registry information
Important dates
- Study start
- 2015
- Primary completion
- 2015
- Study completion
- 2016
- First posted
- May 13, 2015
- Registry last updated
- Aug 26, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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.