Therapeutic Drug MonitoringTANDEMNCT04132115
Optimized Antibiotic Therapy in Patients With Subarachnoid Haemorrhage (ES) and Cerebral Haemorrhage (EC)
An observational study of Therapeutic Drug Monitoring and Subarachnoid Hemorrhage, run by Azienda Sanitaria-Universitaria Integrata di Udine at 2 sites in Italy.
Trial summary
A recent prospective observational clinical study conducted in an intensive care unit of a third level US university hospital showed that 94% of patients with ES and 50% of those with EC had an ARC for a duration of at least one day during the hospital stay. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Therapeutic Drug Monitoring, Subarachnoid Hemorrhage, Intracerebral Hemorrhage
- What is being tested?
- Piperacillin/tazobactam, Meropenem and Daptomycin
- How many people
- 104 participants
- Where
- 2 sitesItaly
- Study dates
- 1 Oct 2019to Oct 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: Patients admitted to the ICU due to intracranial haemorrage or subaracnoid haemorrage
Who may be able to join
- Patients of both sexes > 18 years admitted for ES or EC
- Patients to which one or more water-soluble antibiotics, antifungals or antivirals subject of the present study are prescribed
- Patients who present ARC
Who cannot join
- Patients in whom the plasma samples are contaminated
- Patients in whom the plasma samples are performed in a way that does not comply with the prepared company protocol.
- Patients with BMI < 18 kg / m2.
- Patients with a serum creatinine > 1.4 mg / dL at entry
- Pregnant patients.
Trial locations and contacts
2 sites in 1 country.
Italy2 sites, 2 recruiting
- Recruiting
Anesthesiology and Intensive Care Clinic - Department of Medicine - ASUIUD
Udine, 33100
Luigi Vetrugno, Doctor, +393382873386, luigi.vetrugno@asuiud.sanita.fvg.it
Tiziana Bove, Professor, +393474785763, tiziana.bove@asuiud.sanita.fvg.it
- Not yet recruiting
Terapia Intensiva 1
Udine, 33100
Cristian Deana, MD
About this study
Official title: Prospective Study Evaluating Plasma Exposure of Optimized Antibiotic Therapy According to TDM in Patients With Subarachnoid Haemorrhage (ES) and Cerebral Haemorrhage (EC)
A recent prospective observational clinical study conducted in an intensive care unit of a third level US university hospital showed that 94% of patients with ES and 50% of those with EC had an ARC for a duration of at least one day during the hospital stay.
Although there is currently a great deal of evidence describing ARC in various subgroups of critically ill patients, on the other hand there is little documentation regarding the effect that ARC can have on exposure to renally eliminated drugs.
Therefore, the aim of this study is to prospectively evaluate the proportion of plasma under-exposure to hydrophilic antimicrobials in patients with ES or EC and with ARC, in order to verify whether the recommended dosage regimens for these drugs are adequate for reaching the pharmacodynamic targets of therapeutic efficacy.
Read the detailed description
Haemorrhagic stroke is a devastating disease with a high rate of disability and mortality. In addition to the direct effects of the haemorrhagic event and to the secondary neurological complications, patients with haemorrhagic strokes are predisposed to medical complications that can have a direct impact on both clinical outcome and treatment costs. It has been estimated that between 79% and 100% of patients with subarachnoid haemorrhage (ES) and cerebral haemorrhage (EC) have at least one of these complications. Among them, the most common are infections, seizures, hyponatremia, hypomagnesemia, hypokalemia and venous thromboembolism.
A possible reason that can be responsible for such a high frequency of complications, especially infectious, can be identified in a pathophysiological alteration of the circulatory and renal haemodynamics of this population. Specifically, these patients frequently have a hyperdynamic state which results in a high renal clearance (CrCl) (augmented renal clearance - ARC, defined as a measured CrCl ≥ 130 ml/min/1.73m2). In this regard, a recent prospective observational clinical study conducted in an intensive care unit of a third level US university hospital showed that 94% of patients with ES and 50% of those with EC had an ARC for a duration of at least one day during the hospital stay.
In consideration of the fact that the ARC has been historically underestimated and that an accurate assessment of renal function through the measured CrCl is not regularly carried out on all patients even if they are critical, the main risk from the point of view of therapeutic appropriateness is that of not adjust the dosing regimen of drugs eliminated through the kidney in relation to the presence and extent of the ARC. Moreover, the clinician often ignores the time course of the ARC as well as the modalities with which to carry out the dosage adjustment. This could lead to sub-therapeutic concentrations for renally excreted drugs, as typically are water-soluble antibiotics such as beta-lactams, aminoglycosides, daptomycin, linezolid, antifungal fluconazole and antivirals ganciclovir and aciclovir, resulting in an increase in the risk of therapeutic failure.
Although there is currently a great deal of evidence describing ARC in various subgroups of critically ill patients, on the other hand there is little documentation regarding the effect that ARC can have on exposure to renally eliminated drugs.
Therefore, the aim of this study is to prospectively evaluate the proportion of plasma under-exposure to hydrophilic antimicrobials in patients with ES or EC and with ARC, in order to verify whether the recommended dosage regimens for these drugs are adequate for reaching the pharmacodynamic targets of therapeutic efficacy.
- Being tested
- Piperacillin/tazobactam, Meropenem, Daptomycin, Ceftobiprole, Linezolid
- Keywords
- Intracerebral Hemorrhage, Subarachnoid Hemorrhage, Therapeutic Drug Monitoring
- Medical subject headings
- Subarachnoid Hemorrhage, Cerebral Hemorrhage
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Piperacillin/tazobactamDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
MeropenemDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
DaptomycinDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
CeftobiproleDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
LinezolidDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
VancomycinDrug
Therapeutic drug monitoring(TDM) of this antibiotic plasma concentration
FluconazolDrug
Therapeutic drug monitoring (TDM) of this antifungal plasma concentration
AcyclovirDrug
Therapeutic drug monitoring (TDM) of this antiviral plasma concentration
GentamicinsDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
AmikacinDrug
Therapeutic drug monitoring (TDM) of this antibiotic plasma concentration
GanciclovirDrug
Therapeutic drug monitoring (TDM) of this antiviral plasma concentration
What is being measured
The primary outcome is the main question the study is designed to answer.
Underexposure to antimicrobial therapy
Prospective evaluation of the proportion of plasma underexposure to hydrophilic antimicrobials due to ARC in patients with subarachnoid haemorrhage (ES) and / or cerebral haemorrhage (EC).
Measured: 2 years from the date of approval
Secondary outcomes (3)
T > MIC
Evaluation of the achievement of the pharmacokinetic / pharmacodynamic target of therapeutic efficacy through the calculation of the parameter T > MIC
Measured: 2 years from the date of approval
AUC / MIC
Evaluation of the achievement of the pharmacokinetic / pharmacodynamic target of therapeutic efficacy through the calculation of the parameter AUC / MIC
Measured: 2 years from the date of approval
Performance of ClCr estimation formulas
Evaluation of the performance of the common CrCl estimation formulas compared to the CrCl measured in the estimation of the systemic clearance of the drugs being studied
Measured: 2 years from the date of approval
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Oct 2019
- Study start1 Oct 2019
- Primary completionOct 2021 (estimated)
- Study completionOct 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Therapeutic Drug MonitoringStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 104 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Azienda Sanitaria-Universitaria Integrata di Udine
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Luigi Vetrugno, Azienda Sanitaria-Universitaria Integrata di Udine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04132115
- Sponsor's protocol ID
- CEUR-2019-Os-162
- Acronym
- TANDEM
- Status last verified
- Jul 2021
- First submitted
- 14 Oct 2019
- Last updated
- 21 Jul 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Database will be available upon reasonable request
Study at a glance
From the registry record, last updated by the sponsor on 21 Jul 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prospective Study Evaluating Plasma Exposure of Optimized Antibiotic Therapy According to TDM in Patients With Subarachnoid Haemorrhage (ES) and Cerebral Haemorrhage (EC)
- ClinicalTrials.gov ID
- NCT04132115
- Acronym / sponsor ID
- TANDEM / CEUR-2019-Os-162
- Keywords
- Intracerebral Hemorrhage, Subarachnoid Hemorrhage, Therapeutic Drug Monitoring
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 104 participants (estimated)
- Lead sponsor
- Azienda Sanitaria-Universitaria Integrata di UdineUniversity, hospital or other
- Study start
- 1 Oct 2019 (actual)
- Primary completion
- Oct 2021 (estimated)
- Study completion
- Oct 2021 (estimated)
- First posted
- 18 Oct 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A recent prospective observational clinical study conducted in an intensive care unit of a third level US university hospital showed that 94% of patients with ES and 50% of those with EC had an ARC for a duration of at least one day during the hospital stay.
Although there is currently a great deal of evidence describing ARC in various subgroups of critically ill patients, on the other hand there is little documentation regarding the effect that ARC can have on exposure to renally eliminated drugs.
Therefore, the aim of this study is to prospectively evaluate the proportion of plasma under-exposure to hydrophilic antimicrobials in patients with ES or EC and with ARC, in order to verify whether the recommended dosage regimens for these drugs are adequate for reaching the pharmacodynamic targets of therapeutic efficacy.
Detailed description
Haemorrhagic stroke is a devastating disease with a high rate of disability and mortality. In addition to the direct effects of the haemorrhagic event and to the secondary neurological complications, patients with haemorrhagic strokes are predisposed to medical complications that can have a direct impact on both clinical outcome and treatment costs. It has been estimated that between 79% and 100% of patients with subarachnoid haemorrhage (ES) and cerebral haemorrhage (EC) have at least one of these complications. Among them, the most common are infections, seizures, hyponatremia, hypomagnesemia, hypokalemia and venous thromboembolism.
A possible reason that can be responsible for such a high frequency of complications, especially infectious, can be identified in a pathophysiological alteration of the circulatory and renal haemodynamics of this population. Specifically, these patients frequently have a hyperdynamic state which results in a high renal clearance (CrCl) (augmented renal clearance - ARC, defined as a measured CrCl ≥ 130 ml/min/1.73m2). In this regard, a recent prospective observational clinical study conducted in an intensive care unit of a third level US university hospital showed that 94% of patients with ES and 50% of those with EC had an ARC for a duration of at least one day during the hospital stay.
In consideration of the fact that the ARC has been historically underestimated and that an accurate assessment of renal function through the measured CrCl is not regularly carried out on all patients even if they are critical, the main risk from the point of view of therapeutic appropriateness is that of not adjust the dosing regimen of drugs eliminated through the kidney in relation to the presence and extent of the ARC. Moreover, the clinician often ignores the time course of the ARC as well as the modalities with which to carry out the dosage adjustment. This could lead to sub-therapeutic concentrations for renally excreted drugs, as typically are water-soluble antibiotics such as beta-lactams, aminoglycosides, daptomycin, linezolid, antifungal fluconazole and antivirals ganciclovir and aciclovir, resulting in an increase in the risk of therapeutic failure.
Although there is currently a great deal of evidence describing ARC in various subgroups of critically ill patients, on the other hand there is little documentation regarding the effect that ARC can have on exposure to renally eliminated drugs.
Therefore, the aim of this study is to prospectively evaluate the proportion of plasma under-exposure to hydrophilic antimicrobials in patients with ES or EC and with ARC, in order to verify whether the recommended dosage regimens for these drugs are adequate for reaching the pharmacodynamic targets of therapeutic efficacy.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Patients admitted to the ICU due to intracranial haemorrage or subaracnoid haemorrage
Key inclusion criteria (3 listed)
- Patients of both sexes > 18 years admitted for ES or EC
- Patients to which one or more water-soluble antibiotics, antifungals or antivirals subject of the present study are prescribed
- Patients who present ARC
Key exclusion criteria (5 listed)
- Patients in whom the plasma samples are contaminated
- Patients in whom the plasma samples are performed in a way that does not comply with the prepared company protocol.
- Patients with BMI < 18 kg / m2.
- Patients with a serum creatinine > 1.4 mg / dL at entry
- Pregnant patients.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Piperacillin/tazobactamTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| MeropenemTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| DaptomycinTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| CeftobiproleTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| LinezolidTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| VancomycinTherapeutic drug monitoring(TDM) of this antibiotic plasma concentration | Drug | – |
| FluconazolTherapeutic drug monitoring (TDM) of this antifungal plasma concentration | Drug | – |
| AcyclovirTherapeutic drug monitoring (TDM) of this antiviral plasma concentration | Drug | – |
| GentamicinsTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| AmikacinTherapeutic drug monitoring (TDM) of this antibiotic plasma concentration | Drug | – |
| GanciclovirTherapeutic drug monitoring (TDM) of this antiviral plasma concentration | Drug | – |
Primary outcome
Underexposure to antimicrobial therapy
Time frame: 2 years from the date of approval
Prospective evaluation of the proportion of plasma underexposure to hydrophilic antimicrobials due to ARC in patients with subarachnoid haemorrhage (ES) and / or cerebral haemorrhage (EC).
3 secondary outcomes
T > MIC
Time frame: 2 years from the date of approval
AUC / MIC
Time frame: 2 years from the date of approval
Performance of ClCr estimation formulas
Time frame: 2 years from the date of approval
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Jul 2021.
- Individual participant dataSharing planned: Yes. Database will be available upon reasonable request
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Therapeutic Drug Monitoring and Subarachnoid Hemorrhage, run by Azienda Sanitaria-Universitaria Integrata di Udine at 2 sites in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 21 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact TIZIANA BOVE, MD, AP (+390432555501, TIZIANA.BOVE@UNIUD.IT), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Underexposure to antimicrobial therapy (time frame: 2 years from the date of approval). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2021.