Trials / Enrolling By Invitation
Enrolling By InvitationNCT05156437
Postoperative Antibiotic Management Duration Following Surgery for Intravenous Drug Abuse (IVDA) Endocarditis (OPTIMAL)
- Status
- Enrolling By Invitation
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Vinay Badhwar · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the safety and compliance of initial intravenous (IV) antibiotics followed by oral antibiotic therapy following uncomplicated IVDA endocarditis. Endocarditis has a high rate of sickness and death, involves a long hospitalization and a long-term use of IV antibiotics necessitating six (6) weeks of in-patient hospital stay, and comes with a high cost.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Amoxycillin, Cefalexin, Dicloxacillin, Linezolid, Levofloxacin, Rifampicin | Amoxycillin, Cefalexin, Dicloxacillin, Linezolid, Levofloxacin, Rifampicin |
| DRUG | Ampicillin, Oxacillin, Vancomycin, Daptomycin, Ceftriaxone, Cefepime, Ceftaroline | Ampicillin, Oxacillin, Vancomycin, Daptomycin, Ceftriaxone, Cefepime, Ceftaroline |
Timeline
- Start date
- 2022-03-16
- Primary completion
- 2024-10-01
- Completion
- 2024-10-01
- First posted
- 2021-12-14
- Last updated
- 2023-12-07
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05156437. Inclusion in this directory is not an endorsement.