Blood Pressure Clinical Trial
Official title:
Etude Prospective Observationnelle Multicentrique Sur Volontaires Sains Des VALeurs de Pression Artérielle mesurées Sur Trois Sites alteRnAtIfS Des Membres inférieurs cOmparées au Site de référence
Non-invasive measurement of blood pressure is an instrument governed nursing routine care.
The use of an automated oscillometric cuff is a common technique and validated if this is
done on the arm with a suitable cuff, positioned opposite the brachial artery and up to the
right atrium (the brachial site) . If cons-indication to use the brachial site, measurements
are frequently performed at the ankle, calf or thigh. Among the blood pressure values
measured on the 3 sites of the lower limb (thigh, calf or ankle), it may be a specific
property of which the observed values are closest to the reference values (brachial).
The objective of this study is to measure the non-invasive blood pressure values at three
sites of the lower limb, to compare the reference value to determine which alternative site
should be preferred when the reference measurement is not feasible .
We want to determine the alternative site to obtain values as close as the measured values of
the reference site. The three study sites are the thigh, calf and ankle. The reference site
recommended for monitoring non-invasive blood pressureis the arm.
It is also assessing the impact of certain parameters on the primary endpoint:
- Physiological parameters: gender, weight, height, age, systolic blood pressure
reference, listed measures.
- A parameter related to measurement: discomfort felt when the blood pressure outlet.
- Exposure setting: smoking.
Primary Outcome: The difference in systolic blood pressure, diastolic and mean simultaneously
measured in the arm and each of the three sites in the lower limb.
Secondary endpoints: The difference in systolic blood pressure, diastolic and mean
simultaneously measured in the arm and each of the three sites in the lower limb in the
following subgroups:
- Male / Female
- BMI <25 / BMI> 25
- Size < 160 cm / size [160-169] cm / size [170-180] cm / size [181-190] cm / size ≥ 191
cm
- Age <25 years / age ≥ 25 years
- Systolic Blood Pressure value (SAP) the reference site <100 mmHg / 100 mmHg and ≥ NOT
value of the reference site <140 mmHg / ≥ 140 mmHg
- Visual Analog Scale of discomfort ≤ 4/10 /> 4/10
- Hemibody studied Right / Left
- Smoking / No Smoking
Discomfort level depending on the measurement site of blood pressure in the general
population.
- Discomfort level for each measurement of blood pressure site in each of the following
subgroups:
- Male / Female - BMI <25 / BMI> 25
- size <160 cm / size [160-169] cm / size [170 -180] cm / size [181-190] cm / size ≥ 191
cm - Age <25 / age ≥ 25 years
- blood pressure value (SAP) reference site <100 mmHg / 100 mmHg and ≥ NOT Value reference
site <140 mmHg / ≥ 140 mmHg
- hemibody studied Right / Left
- Smoking / No Smoking
Methodology:
Experimental design:
This is an observational study, prospective, multicenter, comparative on healthy volunteers,
each individual is his own witness. Reports of non-invasive blood pressure values of 3
different sites of the lower limbs, compared to a reference value. For each individual, the
side which will be carried out blood pressure measurements will be drawn. After 5 minutes
rest in the supine position, it will be realized the measurement of blood pressure
non-invasively systolic, mean and diastolic 2 automated oscillometric measuring devices
identical and calibrated simultaneously the arm and thigh ipsilateral / arm and calf
ipsilateral / arm and the ipsilateral ankle.
Each measurement is repeated once after 1 minute.
Statistical analysis:
Systolic, mean and diastolic pressures are analyzed separately, and expressed by their
average with standard deviation and 95% confidence intervals. The concordance of BP
measurements between the arm and each of three sites in the lower limb was analyzed by the
method Bland and Altman, calculating the average difference, its approval limits, as well as
the confidence interval 95 % upper and lower limits of approval subject to a Gaussian
distribution of the difference between the measurements.
The search for the best AP measurement site to the lower member is made by comparing the
differences between each of the three sites and the reference site, for a global test
(variance analysis or test Friedmann according to the distribution of differences), then by
comparisons with 2-2 adjusting the p-value.
The chosen site is one for which this difference is significantly weaker. All tests are
conducted bilaterally with a risk of first species set at 5%. In an earlier study, the
largest variance found regarding the difference in systolic BP between calf and arm.
Based on the most pessimistic scenario (s = 12.76) to highlight a difference of 5 mm Hg with
an alpha risk of 5% and a power of 90% and taking into account the multiple comparisons
considered, 176 patients necessary.
Total duration of study: 27 months Period of inclusion: 24 months Duration of participation
for voluntary: 30 minutes Number of participating centers: 8 centers
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