Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05156437 · ClinicalTrials.gov registry record · Phase 4

Postoperative Antibiotic Management Duration Following Surgery for Intravenous Drug Abuse (IVDA) Endocarditis (OPTIMAL)

A Phase 4 study, sponsored by West Virginia University.

Terminated
Registry status
Phase 4
Development phase
5
Enrollment target

NCT05156437 is a Phase 4 study that was terminated before completion, run by West Virginia University. The registered enrollment target is 5 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05156437, a Phase 4 study, was terminated before completion, sponsored by West Virginia University.

TERMINATED
Registry status
Phase 4
Development phase
5 participants
Enrollment target

Study 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.

Interventions

  • DRUG Amoxycillin, Cefalexin, Dicloxacillin, Linezolid, Levofloxacin, Rifampicin
  • DRUG Ampicillin, Oxacillin, Vancomycin, Daptomycin, Ceftriaxone, Cefepime, Ceftaroline

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2022-03-16
Est. Completion 2024-10-31
Phase Phase 4

Sponsor

West Virginia University

122 total trials

What the Registry Record Tells You About NCT05156437

The ClinicalTrials.gov registry entry for NCT05156437 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is West Virginia University, which has 122 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Amoxycillin, Cefalexin, Dicloxacillin, Linezolid, Levofloxacin, Rifampicin is the first listed.

NCT05156437 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05156437 about?

NCT05156437 is a clinical study titled "Postoperative Antibiotic Management Duration Following Surgery for Intravenous Drug Abuse (IVDA) Endocarditis (OPTIMAL)". 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 ant...

What is the current status of trial NCT05156437?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 5 participants. The study started on 2022-03-16. Estimated completion is 2024-10-31.

What interventions are being tested in trial NCT05156437?

The interventions under investigation include: Amoxycillin, Cefalexin, Dicloxacillin, Linezolid, Levofloxacin, Rifampicin (DRUG), Ampicillin, Oxacillin, Vancomycin, Daptomycin, Ceftriaxone, Cefepime, Ceftaroline (DRUG).

Who is sponsoring clinical trial NCT05156437?

This trial is sponsored by West Virginia University, which has 122 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.