Administration of Subcutaneous Teicoplanin in the Treatment of

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

See also
Status	Clinical Trial	Phase
Completed	`NCT01500837` - Treatment of Methicillin-sensitive Staphylococcus Aureus (MSSA)	N/A
Recruiting	`NCT05046860` - Efficacy of Dalbavancin in Osteoarticular Infections Associated With Hip and Knee Replacements	N/A
Completed	`NCT02599493` - EVRIOS : Comparative Evaluation of Low Versus High Doses of Rifampicin	Phase 4

See also

Status

Clinical Trial

Phase

Completed

NCT01500837 - Treatment of Methicillin-sensitive Staphylococcus Aureus (MSSA)

N/A

Recruiting

NCT05046860 - Efficacy of Dalbavancin in Osteoarticular Infections Associated With Hip and Knee Replacements

N/A

Completed

NCT02599493 - EVRIOS : Comparative Evaluation of Low Versus High Doses of Rifampicin

Phase 4

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01815541
Study type	Interventional
Source	Centre Hospitalier Universitaire, Amiens
Contact
Status	Completed
Phase	Phase 2
Start date	March 2013
Completion date	July 2015

Administration of Subcutaneous Teicoplanin in the Treatment of Osteoarticular Infections: Tolerance Study — TEICOPLANIN

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms