Trials / Completed
CompletedNCT06592547
Intravenous Metoprolol in Septic Shock
EFFECT of INTRAVENOUS METOPROLOL TARTRATE on MORTALITY in PATIENTS with SEPTIC SHOCK DUE to VENTILATOR-ASSOCIATED PNEUMONIA Thesis
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Alexandria University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A RCT designed to assess the effect of giving intravenous beta-blockers in patients with septic shock after achieving hemodynamic stability. The principle of this study is to control heart rate allowing for better diastolic filling and thus better perfusion.
Detailed description
A RCT, conducted at alexandria main university hospital, patients were divided into 2 groups, Control group which received the standard care for septic shock and metoprolol group which recieved intravenous metoprolol then patients were assessed for Blood pressure, heart rate, iv fluids needed, vasopressor doses and 28 days mortality
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Intravenous metoprolol tartrate | An intravenous beta-blockers, recieved FDA approval |
| OTHER | Standard Care (in control arm) | Standard care according to surviving sepsis campaign |
Timeline
- Start date
- 2022-04-01
- Primary completion
- 2023-12-01
- Completion
- 2024-11-10
- First posted
- 2024-09-19
- Last updated
- 2025-01-29
Locations
1 site across 1 country: Egypt
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06592547. Inclusion in this directory is not an endorsement.