Evaluation of Pharmacokinetic / Pharmacodynamic and Tolerance Assessment of Dermal Administration of Beta-lactams in the Elderly
NCT ID: NCT02897648
Last Updated: 2023-03-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
2 participants
OBSERVATIONAL
2015-06-26
2023-03-06
Brief Summary
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This is an alternative to oral, sublingual, rectal or intravenous Many drugs are used by subcutaneous route but few clinical studies evaluating the level of scientific relevance justifies their use.
The purpose of this study is to assess:
1. / Determine that there is no difference between the subcutaneously compared to intravenous administration in terms of dosage and serum PK / PD of Beta lactam objectives in a geriatric population.
2. / The safety and lack of toxicity of administrations subcutaneously.
Advantages disadvantages
* easy Of establishment
* Simplicity Monitoring and manipulation
* Reduced Risk of infection
* No Risk of venous thrombosis
* Lower cost Simple -Technique for support at home taking
* Limitation Aggressive gestures
* multiplicity Of all possible injection sites
* Technique Of choice for agitated patients or confused -Risk of localized edema (\<1000mL / 24 / site)
* Use Impossible for some drugs
* Risk Discomfort and intolerance at the injection site
A practical study was conducted among 382 physicians (289 geriatricians and 93 infectious disease specialists). Among them 97.5% reported regular use of the subcutaneous route for the administration of antibiotics.
Declarative criteria pretend curb the use of this route was the lack of data Pk / Pd (61.2%); the absence of marketing authorization for the subcutaneous route (34.5%); the absence of serum assay available (2.1%).
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Detailed Description
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Primary objective :
• Determine that there is no difference between the subcutaneously compared to intravenous administration in terms of dosage and serum PK / PD objectives Beta lactam in a geriatric population.
Secondary objectives:
* Clinical evaluation at J14 and J90 (healing, death)
* Clinical tolerance of subcutaneously by self-assessment or hetero-evaluation of the existence of cognitive disorders
Monitoring of antibiotic dosages:
* Making systematic assay serum concentrations of residual antibiotics in the range of 30 min prior to reinjection H24 after starting treatment and then weekly monitoring.
* Realization of the assays according to the method of Liquid Chromatography-Mass Spectrometry (LC-MS)
Patient monitoring of J1-J14:
• Clinical monitoring and biological usual
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Assessment of dermal administration of Beta-Lactams
Evaluation of Pharmacokinetic / Pharmacodynamic of dermal administration of Beta-Lactams
Eligibility Criteria
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Inclusion Criteria
* Infection may cause bacteremia or not: Gram-negative bacilli and gram-positive cocci susceptible to beta-lactam
Exclusion Criteria
* polymicrobial infection
75 Years
ALL
No
Sponsors
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Fondation Hôpital Saint-Joseph
OTHER
Responsible Party
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Principal Investigators
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EL HELALI Najoua, MD
Role: PRINCIPAL_INVESTIGATOR
Fondation Hôpital Saint-Joseph
Locations
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Groupe Hospitalier Paris Saint Joseph
Paris, Île-de-France Region, France
Countries
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Other Identifiers
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BETALACUTANE
Identifier Type: -
Identifier Source: org_study_id
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