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RCT study on the efficacy evaluation of pituitrin in the treatment of vasoparsy syndrome after cardiopulmonary bypass :

RCT study on the efficacy evaluation of pituitrin in the treatment of vasoparsy syndrome after cardiopulmonary bypass :

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082166
Enrollment
Unknown
Registered
2024-03-22
Start date
2023-10-19
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

vasoplegic syndrome

Interventions

Posterior pituitary hormone group:Posterior pituitary hormones

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age =18 years old, gender is not limited; (2) high-risk and severe (LVEF <50%) cardiac CPB within 24h, after adequate rehydration, there are still ? mean arterial pressure (MAP) <70mmHg; ? cardiac output index (CI) =2.5L/min/m²; ? SVRI =1200 dyn-sec/cm5/m²; ? central venous pressure (CVP) <5mmHg; ? pulmonary capillary wedge pressure ( PCWP<10mmHg; the above conditions must be satisfied at the same time; (3) Agree to sign the study informed consent form.

Exclusion criteria

Exclusion criteria: 1) Age< 18 years old; 2) preoperative co-infection; 3) presence of acute coronary syndrome before surgery; 4) malignant arrhythmia (ventricular tachycardia, ventricular fibrillation) occurred before surgery; 5) acute mesenteric ischemia before surgery; 6) preoperative renal replacement therapy; 7) Presence of endocrine or peripheral vascular disease (Raynaud's disease, etc.) before surgery; 8) the presence of other ventricular assist devices other than IABP; 9) have a history of pregnancy and tumors; 10) Refusal to sign the informed consent form for the study.

Design outcomes

Primary

MeasureTime frame
ICU time ;Acute kidney injury ;

Secondary

MeasureTime frame
Acute myocardial infarction ;Arrhythmia;Low cardiac output syndrome;Stroke ;Digital and mesenteric ischemia;Ventilator assist time> 48 hours ;Hospital stay ;Hospital costs ;

Countries

China

Contacts

Public ContactYanbo Zhang

Fuwai Hospital, Chinese Academy of Medical Sciences

yanbozhang@126.com+86 136 0106 6587

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026