Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Vasoactive Agents in Pulmonary Hypertension Crisis

Official title: Comparison of the Efficacy and Safety of Dopamine, Norepinephrine and Epinephrine in the Treatment of Pulmonary Hypertensive Crisis Under Hemodynamic Monitoring

Run by China National Center for Cardiovascular Diseases · NCT07667829 · Data updated 2026-11-12

This trial tests whether dopamine, norepinephrine, or epinephrine can safely and effectively help people with a pulmonary hypertension crisis who are in the hospital.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment75 (estimated)
SponsorChina National Center for Cardiovascular Diseases
Government
Locations3 sites (Beijing, Beijing Municipality and 2 other locations)
StatusRecruiting
StartedAugust 19, 2026
Main results expectedDecember 31, 2028
Study endsJanuary 31, 2029
Registry record updatedOctober 30, 2026
Trial IDNCT07667829 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults over 18 with confirmed PAH or CTEPH who are hospitalized and have not yet received any study vasopressors.

Probably not a fit

Patients not experiencing a pulmonary hypertension crisis or those with contraindications to the study drugs may not benefit.

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

What this trial studies

This prospective, randomized trial compares three vasoactive drugs—dopamine, norepinephrine, and epinephrine—for treating patients experiencing a pulmonary hypertension crisis. Haemodynamic monitoring guides the assessment of each drug’s safety and effectiveness. Eligible adults with PAH or CTEPH who are in hospital and have not yet received any of the study drugs are randomized to receive one of the agents. The study aims to identify which agent provides the best balance of blood pressure support and oxygen delivery while minimizing adverse events. Conducted at major Chinese centers, the trial emphasizes in-hospital management and continuous safety monitoring.

Why it matters

Potential benefit: If successful, the trial could identify the most effective and safe vasopressor strategy for supporting patients during a pulmonary hypertension crisis.

How similar studies have gone: Prior research in similar settings has explored vasoactive drugs, but this study addresses a specific crisis scenario with randomized comparison among three agents.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age \> 18 years old;
2. Signed informed consent form;
3. Confirmed diagnosis of arterial pulmonary hypertension (PAH) and/or chronic thromboembolic pulmonary hypertension (CTEPH);
4. Presenting with manifestations of pulmonary hypertensive crisis;
5. Receiving both diagnosis and treatment in-hospital;
6. No intravenous administration of the vasopressor drugs (including dopamine, norepinephrine, and epinephrine) under study at enrollment.

Exclusion Criteria:

1. At SCAI stage D or stage E ;
2. Patients who only receive a diagnosis but no treatment in the hospital;
3. Uncontrolled hyperthyroidism;
4. Complicated with angle-closure glaucoma;
5. Hypersensitivity to the study drug;
6. Ongoing use of halogenated hydrocarbon general anesthetics such as cyclopropane and halothane;
7. Ongoing use of monoamine oxidase inhibitor (MAOI) antidepressants or anti-Parkinson drugs (phenelzine, tranylcypromine, isocarboxazid, moclobemide);
8. Pregnancy;
9. Already receiving the vasopressor drugs (dopamine, norepinephrine, epinephrine) under study at enrollment.

Where it's running

  • Chinese Academy of Medical Sciences, Fuwai Hospital
    Beijing, Beijing Municipality, China
    Recruiting
  • Guangdong Provincial People's Hospital
    Guangzhou, Guangdong, China
    Not yet recruiting
  • Zhongnan Hospital of Wuhan University
    Wuhan, Wuhan, China
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.