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Continuous versus intermittent noninvasive blood pressure measurement in patients undergoing surgery in the beach-chair position

The influence of the continuous versus intermittent noninvasive blood pressure measurement on hemodynamic stability in patients undergoing surgery in the beach-chair position

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001058864
Enrollment
80
Registered
2012-10-04
Start date
2012-10-14
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Aim of the study is to evaluate the safety and efficacy of the use of a completly noninvasive device enabling the continuous measurement of blood pressure in patients with increased risk of cerebral malperfusion due to position changes (beach-chair position) under general anesthesia in compariosn to the standard anesthesia care. As a measure of safety/eficacy the proportion of time outside the near-normal ranges of blood pressures and hypotensive periods will be used in combination with assesment of mental abilities derrangements in the early postoperative course and potential postoperative morbidity.

Interventions

Maintanace of the near-normal pressure values throughout the surgery in beach-chair position (using fluids and vasopressors) with continuous noninvasive measurement of blood pressure obtained by the CNAP device (volume clamp method).

Sponsors

Dpt. of Anesthesia and Intensive Care of the Faculty of Medicine Plzen - Charles University Prague
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients undergoing surgery in beach-chair position (throid gland surgery, shoulder surgery/arthroscopy) General anesthesia Given and signed informed consent

Exclusion criteria

obvious perfusion abnormality on the side of measurement, vascular implants or known neuronal / neuromuscular disease on the side of measurement, peripheral edema

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026