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 type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Peking Union Medical College Hospital Academic / other |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Status | Recruiting |
| Started | September 1, 2025 |
| Main results expected | July 1, 2027 |
| Study ends | September 1, 2027 |
| Registry record updated | June 17, 2026 |
| Trial ID | NCT07653659 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
- Study coordinator: Bin Du, Dr
- Email: sunyaliii@163.com
- Phone: 86+15136289398
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.