Development and evaluation of a new method to determine baroreflex sensitivity, and its application to clinical investigations

Squatting test-2 - Squatting test-2

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000038088

Enrollment

Registered

2020-01-01

Start date

2020-01-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Healthy volunteers

Interventions

Intravenous access is established, and the blood pressure is increased and decreased by intravenous phenylephrine and nitroprusside, respectively.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: healthy volunteers without medication

Exclusion criteria

Exclusion criteria: Subjects with a history of cardiovascular, respiratory or metabolic disorders are excluded

Design outcomes

Primary

Measure	Time frame
Correlations between baroreflex sensitivity determined by the squatting test vs. those of the Oxford method, spontaneous sequence method, and Valsalva test.	—

Countries

Japan

Contacts

Public ContactMakoto Tanaka

University of Tsukuba, faculty of medicine Department of Anesthesiology

mtanaka@md.tsukuba.ac.jp029-853-3285

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026