Trials / Unknown
UnknownNCT03208257
Esmolol to Control Adrenergic Storm in Septic Shock- ROLL-IN 2
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 10 (estimated)
- Sponsor
- Samuel Brown · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Septic shock is a common syndrome caused by the body's response to an infection. Septic shock is responsible for 10% of all ICU admissions and 30% of ICU deaths. Use of "beta blocker" medications may improve outcomes after septic shock. This pilot study evaluates protocols to infuse the beta blocker esmolol in patients with septic shock.
Detailed description
This is a prospective, single arm, feasibility study of esmolol infusion in septic shock. The objective is to evaluate the feasibility, adequacy, and efficiency of study protocols for a subsequent ECASSS study. This study (ECASSS-R2) extends observations made in an initial pilot, ECASSS-R.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Esmolol | Esmolol hydrochloride infusion |
Timeline
- Start date
- 2017-08-07
- Primary completion
- 2020-12-01
- Completion
- 2021-06-01
- First posted
- 2017-07-05
- Last updated
- 2019-02-26
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03208257. Inclusion in this directory is not an endorsement.