Clinical Trials Directory

Trials / Unknown

UnknownNCT02842983

Pilot Study: Echocardiographic and Hemodynamic Effects of Esmolol in Septic Shock Patients

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
36 (estimated)
Sponsor
Peking Union Medical College Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

After initial hemodynamic stabilization, 36 septic shock patients with heart rate \> of 90 bpm and requiring norepinephrine to maintain mean arterial pressure (MAP) more than 65 mmHg will be randomised into two groups, esmolol group and control group. Patients allocated to esmolol group will receive a continuous esmolol infusion to maintain a lowering of heart rate of 10%. Norepinephrine will be titrated to achieve a MAP more than 65 mmHg. To investigate myocardial performance, the investigators will assess Tissue Doppler imaging by echocardiography and hemodynamic measures. Data will be obtained at baseline ,after esmolol infusion once achieved the predefined heart rate threshold and 72hours after esmolol infusion.

Detailed description

primary outcome were determined according to our previous study of tissue doppler.

Conditions

Interventions

TypeNameDescription
DRUGEsmololconventional management plus esmolol infusion

Timeline

Start date
2014-12-01
Primary completion
2016-12-01
Completion
2016-12-01
First posted
2016-07-25
Last updated
2016-07-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02842983. Inclusion in this directory is not an endorsement.

Pilot Study: Echocardiographic and Hemodynamic Effects of Esmolol in Septic Shock Patients (NCT02842983) · Clinical Trials Directory