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Influence of Dopamine and Noradrenaline on Hemodynamic Parameters in Patients with Postpartum Hemorrhage

Influence of Dopamine and Noradrenaline on Hemodynamic Parameters in Patients with Postpartum Hemorrhage

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003918
Enrollment
Unknown
Registered
2013-11-27
Start date
2013-12-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

postpartum hemorrhage

Interventions

dopamine:accept the dopamine treatment (DA group), which could be increased to a maximum dose of 20ug/kg/min.
noradrenaline:accept the norepinephrine treatment (NE Group) randomly, which could be increased rapidly to a maximum dose of 0.20ug/kg/min

Sponsors

ICU, Beijing Tiantan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Postpartum patients older than 18 years old; 2. Patients who conform to the diagnostic criteria of postpartum hemorrhage and after actively etiological treatment and adequate fluid resuscitation hemodynamics is still unstable also need vasoactive drugs; 3. Patients who are given mechanical ventilation; 4. Patents in the ICU; 5. Patients with PiCCO monitoring.

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to sign the informed consent or who have signed the informed consent but quit in the research process; 2. Patients with serious heart diseases such as: cardiomyopathy and congenital heart disease; 3. Patients with primary pulmonary hypertension; 4. Patients with pregnancy associated with kidney failure; 5. Patients administered with dopamine or norepinephrine for less than 6 hours, while the combination of vasoactive drugs or surgery treatment is needed; 6. Patients with missed important data. Patients who fail to set and maintain a central venous catheter as planned, or whose Picco monitoring or blood gas examination has not been conducted.

Design outcomes

Primary

MeasureTime frame
stroke volume;vascular resistance index (SVRI);global end diastolic volume index (GEDI);the duration of ventilatory support;

Secondary

MeasureTime frame
lactic acide;

Countries

China

Contacts

Public ContactJianxin Zhou

Daxing Teaching Hospital of Capital Medical University

zhoujx.cn@gmail.com+86 13801183875

Outcome results

None listed

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