Trials / Completed
CompletedNCT04730856
Standard vs High Prophylactic Doses or Anticoagulation in Patients With High Risk of Thrombosis Admitted With COVID-19 Pneumonia (PROTHROMCOVID)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 311 (actual)
- Sponsor
- Hospital Universitario Infanta Leonor · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The main objective is to evaluate the efficacy and safety of three doses of tinzaparin (prophylactic, intermediate and therapeutic) in hospitalized patients with COVID-19 pneumonia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Tinzaparin | day subcutaneously • Follow-up phase 1 (Day 15 to day 30): The information is obtained at discharge and on day +14, + 28 on 30 days. The latter information is obtained from patients, from medical records or by telephone contact at the patient's home. • Follow-up phase 2 (At 3 months: Information is obtained from patients, medical records, or by telephone contact at the patient's home. |
Timeline
- Start date
- 2021-02-01
- Primary completion
- 2021-10-20
- Completion
- 2021-12-20
- First posted
- 2021-01-29
- Last updated
- 2022-09-15
Locations
18 sites across 1 country: Spain
Source: ClinicalTrials.gov record NCT04730856. Inclusion in this directory is not an endorsement.