Clinical trial Recruiting at 1 site Observational Ages 18 and up

Norepinephrine Dose Reduction and Critical Closing Pressure in Distributive Shock

Official title: Changes in Critical Closing Pressure and Derived Hemodynamic Parameters Following Norepinephrine Dose Reduction in Distributive Shock Patients: a Prospective Observational Study

Run by Peking Union Medical College Hospital · NCT07653659 · Data updated 2026-11-12

This study tests how lowering norepinephrine in mechanically ventilated distributive shock patients affects critical closing pressure and related hemodynamic measures.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorPeking Union Medical College Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedSeptember 1, 2025
Main results expectedJuly 1, 2027
Study endsSeptember 1, 2027
Registry record updatedJune 17, 2026
Trial IDNCT07653659 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with distributive shock on norepinephrine, mechanically ventilated, MAP 75–85 mmHg, with a PiCCO catheter, and in whom clinicians plan a norepinephrine dose reduction.

Probably not a fit

Patients with unstable hemodynamics or conditions requiring ongoing high-dose vasoactive support may derive no benefit from || or be excluded from interpretation of hemodynamic changes.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this observational study, clinicians reduce norepinephrine dose for eligible adults with distributive shock who are on MAP 75–85 mmHg and have a PiCCO catheter. Hemodynamic parameters, including critical closing pressure (Pcc), tissue perfusion pressure (TPP), mean systemic filling pressure analogue (Pmsf), and vascular waterfall (VW), are measured at baseline and about 30 minutes after dose reduction during controlled inspiratory holds. The approach relies on stepwise inspiratory hold maneuvers to derive Pcc from CO-MAP regression, ensuring stability by keeping MAP variation under 5 mmHg. No investigator-initiated intervention is performed beyond observing real-world dose reductions by the treating team.

Why it matters

Potential benefit: If successful, findings could improve understanding of how norepinephrine adjustments influence tissue perfusion and vascular dynamics in distributive shock.

How similar studies have gone: Previous work has explored hemodynamic effects of vasoactive changes, but this study adds prospective observation of Pcc and derived metrics in the context of real-world dose reductions.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Adult distributive shock patients aged ≥18 years;
2. Receiving norepinephrine infusion with MAP in the 75-85 mmHg range;
3. PiCCO catheter in situ;
4. Under mechanical ventilation;
5. Clinically indicated norepinephrine dose reduction per attending physician judgment.

Exclusion Criteria:

1. Significant cardiac arrhythmia affecting CO measurement reliability;
2. Contraindication to airway plateau pressure maneuver;
3. Active titration of other vasoactive agents within 30 minutes prior to measurement;
4. Hemodynamic instability making it impossible to reduce norepinephrine dose.

Where it's running

  • Peking Union Medical College Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.