Pharmacokinetics Ertapenem Burns

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT02872272` - Amikacin Pharmacokinetic Profile in Plasma and Tissue After an Administration Using Impregnated Dressings in Burned Patient Population	Phase 4
Completed	`NCT02549079` - Soluble Factors in the Serum of Severely Burned Patients	N/A
Completed	`NCT03742648` - The Effectiveness of Deep Breathing Exercises and Incentive Spirometry in Second Degree Inhalation Burn Patients	N/A

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT02872272 - Amikacin Pharmacokinetic Profile in Plasma and Tissue After an Administration Using Impregnated Dressings in Burned Patient Population

Phase 4

Completed

NCT02549079 - Soluble Factors in the Serum of Severely Burned Patients

N/A

Completed

NCT03742648 - The Effectiveness of Deep Breathing Exercises and Incentive Spirometry in Second Degree Inhalation Burn Patients

N/A

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	NCT01497990
Study type	Interventional
Source	Nantes University Hospital
Contact
Status	Completed
Phase	Phase 4
Start date	January 2010
Completion date	September 2011

Pharmacokinetics Ertapenem Burns

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms