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NCT Number: NCT07609095

Peripheral pULSe Assessment and Arterial pRessure (PULSAR)

This prospective multicenter observational study aims to investigate the relationship between palpable peripheral pulses and simultaneously measured arterial blood pressure in adult patients with circulatory shock or impending circulatory failure. Peripheral pulse palpation is routinely used in emergency medicine, trauma care, critical care, and cardiopulmonary resuscitation as a rapid clinical assessment of circulation. However, the association between palpable pulses and actual arterial blood pressure remains poorly validated.

Patients treated in emergency departments, intensive care units, operating rooms, and other acute care settings will undergo routine pulse palpation at predefined anatomical locations including carotid, femoral, and radial arteries. Simultaneously measured non-invasive and/or invasive arterial blood pressure values will be recorded from routine clinical monitoring systems. Additional clinical variables relevant to circulatory status will also be collected.

The study seeks to define blood pressure thresholds associated with pulse palpability and evaluate the agreement between invasive and non-invasive blood pressure measurements in patients with circulatory shock.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Region Stockholm, all hospitals

Stockholm, Stockholm County, 11883, Sweden

Location status: Recruiting

Location contact

Mattias Günther, MD PhD

CONTACT

[email protected]

46812361000

About this study

The presence or absence of palpable peripheral pulses is widely used as a rapid bedside indicator of circulatory status during trauma care, emergency medicine, intensive care, and cardiopulmonary resuscitation. Advanced Trauma Life Support (ATLS) teaching traditionally assumes that palpable pulses at different anatomical sites correspond to specific systolic blood pressure thresholds. However, these assumptions are based on limited evidence from small observational studies.

This international multicenter prospective observational cohort study aims to investigate the relationship between palpable carotid, femoral, and radial pulses and simultaneously measured arterial blood pressure in adult patients with circulatory shock or impending circulatory failure.

Patients receiving routine hemodynamic monitoring with non-invasive blood pressure (NIBP) and/or invasive arterial blood pressure (IBP) monitoring will be included. Pulse palpation will be performed during routine clinical care without altering treatment or management.

The primary objective is to determine the association between pulse palpability and measured systolic blood pressure. Secondary objectives include identifying blood pressure thresholds associated with pulse palpability, evaluating agreement between invasive and non-invasive blood pressure measurements, and assessing whether patient factors such as vascular disease or vasoactive medication use influence pulse palpability.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical signs of circulatory shock or impending circulatory failure
  • Availability of non-invasive and/or invasive arterial blood pressure monitoring
  • Pulse palpation possible without interfering with emergency care

Exclusion criteria

  • Peripheral vascular conditions preventing reliable pulse palpation
  • Major extremity amputation affecting assessment sites
  • Clinical situations where study procedures interfere with life-saving treatment

Treatment and study plan

Peripheral Pulse Palpation

Procedure

Manual palpation of carotid, femoral, and radial pulses performed during routine clinical care in patients with circulatory instability. Simultaneous arterial blood pressure measurements are recorded from standard monitoring systems. No study-specific treatment or intervention is administered.

Primary outcomes

  1. Association between palpable pulses and systolic arterial blood pressure

    Time frame: During episodes of circulatory instability, up to 24 hours after inclusion

    Relationship between palpable carotid, femoral, and radial pulses and simultaneously measured systolic arterial blood pressure.

Secondary outcomes

  1. Mean arterial pressure associated with pulse palpability

    Time frame: During episodes of circulatory instability, up to 24 hours after inclusion

    Relationship between pulse palpability and mean arterial pressure (MAP).

  2. Agreement between non-invasive and invasive blood pressure measurements

    Time frame: During episodes of circulatory instability, up to 24 hours after inclusion

    Agreement between oscillometric non-invasive blood pressure and invasive arterial blood pressure measurements.

  3. Effect of vascular disease and vasoactive medication on pulse palpability

    Time frame: During hospital admission, up to 30 days

    Influence of peripheral vascular disease, atherosclerosis, age, and vasoactive medications on pulse palpability.

Study contacts

Contact information is provided by the study sponsor or research team.

Mattias Günther, MD PhD

CONTACT

[email protected]

46812361000

Sponsors and collaborators

Lead sponsor

Region Stockholm

Other Gov

Registry information

Official study title

Association Between Palpable Peripheral Pulses and Arterial Blood Pressure in Patients With Circulatory Shock: An International Prospective Multicenter Observational Cohort Study

Acronym: PULSAR

Important dates

Study start
2026
Primary completion
2031
Study completion
2031
First posted
May 27, 2026
Registry last updated
May 27, 2026

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.

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