NCT07609095

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
68mo left

Started Jun 2026

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress1%
Jun 2026Dec 2031

First Submitted

Initial submission to the registry

May 13, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

May 27, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2031

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2031

Last Updated

May 27, 2026

Status Verified

May 1, 2026

Enrollment Period

5 years

First QC Date

May 13, 2026

Last Update Submit

May 19, 2026

Conditions

Keywords

Circulatory ShockHemodynamic MonitoringPulse PalpationPeripheral PulseArterial Blood PressureHypotensionCritical CareTraumaResuscitationHemodynamic Instability

Outcome Measures

Primary Outcomes (1)

  • Association between palpable pulses and systolic arterial blood pressure

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

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

Secondary Outcomes (3)

  • Mean arterial pressure associated with pulse palpability

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

  • Agreement between non-invasive and invasive blood pressure measurements

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

  • Effect of vascular disease and vasoactive medication on pulse palpability

    During hospital admission, up to 30 days

Study Arms (1)

Patients With Circulatory Shock

Adult patients with clinical signs of circulatory shock or impending circulatory failure undergoing routine hemodynamic monitoring with non-invasive and/or invasive arterial blood pressure measurement during standard clinical care.

Procedure: Peripheral Pulse Palpation

Interventions

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.

Patients With Circulatory Shock

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients with circulatory shock or impending circulatory failure treated in emergency departments, intensive care units, operating rooms, trauma centers, and other acute care settings.

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Region Stockholm, all hospitals

Stockholm, Stockholm County, 11883, Sweden

RECRUITING

Related Publications (2)

  • Gunther M, Dahlberg M, Rostami A, Azadali A, Arborelius UP, Linder F, Rostami E. Incidence, Demographics, and Outcomes of Penetrating Trauma in Sweden During the Past Decade. Front Neurol. 2021 Nov 15;12:730405. doi: 10.3389/fneur.2021.730405. eCollection 2021.

    PMID: 34867718BACKGROUND
  • Kim SH, Lilot M, Sidhu KS, Rinehart J, Yu Z, Canales C, Cannesson M. Accuracy and precision of continuous noninvasive arterial pressure monitoring compared with invasive arterial pressure: a systematic review and meta-analysis. Anesthesiology. 2014 May;120(5):1080-97. doi: 10.1097/ALN.0000000000000226.

    PMID: 24637618BACKGROUND

MeSH Terms

Conditions

ShockHypotensionCritical IllnessWounds and Injuries

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsVascular DiseasesCardiovascular DiseasesDisease Attributes

Central Study Contacts

Mattias Günther, MD PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD PhD Associate Professor

Study Record Dates

First Submitted

May 13, 2026

First Posted

May 27, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

June 1, 2031

Study Completion (Estimated)

December 31, 2031

Last Updated

May 27, 2026

Record last verified: 2026-05

Locations