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Pediatric Critical IllnessTACTICNCT07822243

Tissue Penetration of Antibiotics in CriTically Ill Children

An observational study of Pediatric Critical Illness and Critical Illness, run by University Hospital, Ghent at 1 site in Belgium.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This clinical study evaluates the extent to which three commonly administered beta-lactam antibiotics (piperacillin-tazobactam, meropenem, and amoxicillin-clavulanic acid) penetrate tissue in critically ill pediatric patients. Read more about this study

Who is it for?
Ages 1 month to 15 years
Conditions the study is for
Pediatric Critical Illness, Critical Illness
What is being tested?
Pharmacokinetic sampling (Microdialysis and blood sampling)
Type of treatment
Injection or infusion
How many people
60 participants
Where
1 siteBelgium
Study dates
1 Oct 2021to 31 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

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 1 month to 15 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: The study population consists of critically ill pediatric patients aged 1 month to 15 years admitted to the Pediatric Intensive Care Unit (PICU) of Ghent University Hospital who are receiving intravenous therapy with piperacillin-tazobactam, meropenem, or amoxicillin-clavulanic acid for known or suspected severe infection/sepsis. All included patients are under continuous analgosedation and mechanical ventilation at the time of microdialysis catheter placement and have established intra-arterial or intravenous access for routine blood sampling.

Who may be able to join

  • Patient admitted to the Pediatric Intensive Care Unit (PICU).
  • Age: 1 month to 15 years.
  • Receiving intravenous antibiotic treatment with piperacillin-tazobactam, meropenem, or amoxicillin-clavulanic acid.
  • Receiving continuous analgosedation (required for microdialysis catheter insertion; if analgosedation is stopped after insertion, the catheter may remain in place).
  • Intra-arterial (preferred) or intravenous access available for blood sampling.

Who cannot join

  • Presence of coagulopathy and/or thrombocytopenia:
  • Platelet count < 50,000/µL
  • International Normalized Ratio (INR) > 1.5
  • Activated partial thromboplastin time (aPTT) > 1.5 x upper limit of normal value (age-specific thresholds: > 50 sec for 30-90 days; > 42 sec for 90-180 days; > 38 sec for > 180 days)
  • Personal or family history of excessive bleeding.
  • Current treatment with coumarin derivative anticoagulants.
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  • Known hypersensitivity to beta-lactam antibiotics.
  • Pregnancy.
  • Absence of parental (or legal guardian) informed consent.
  • Absence of suitable catheter for blood sampling.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Belgium1 site, 1 recruiting
  • Ghent University Hospital

    Ghent, 9000

    Anca Amza, +32 9 332 18 83, anca.amza@uzgent.be

    Eline Hermans, MD PhD

    Recruiting

Other trials in Belgium

About this study

Official title: TACTIC Study: Tissue Penetration of Antibiotics in CriTically Ill Children

This clinical study evaluates the extent to which three commonly administered beta-lactam antibiotics (piperacillin-tazobactam, meropenem, and amoxicillin-clavulanic acid) penetrate tissue in critically ill pediatric patients.

The primary objectives of this study are to:

Read more
  • Determine whether tissue penetration of beta-lactam antibiotics is impaired in critically ill pediatric patients during initial dosing and steady-state conditions.
  • Evaluate whether antibiotic concentrations within interstitial tissue fluid achieve defined pharmacokinetic and pharmacodynamic targets.
  • Assess the impact of patient demographics and clinical characteristics on antibiotic disposition in muscle tissue.

Investigators will measure unbound antibiotic concentrations in tissue fluid using microdialysis, a technique involving the placement of a microdialysis catheter into the muscle tissue.

Participating patients will undergo the following procedures:

  • Insertion of a flexible microdialysis catheter into the vastus lateralis (thigh) muscle under continuous sedation.
  • Administration of the prescribed antibiotic therapy in accordance with standard medical care.
  • Collection of microdialysate and blood samples across specified dosing intervals to quantify tissue and plasma drug concentrations.
Read the detailed description

Pathophysiological alterations during critical illness, such as severe sepsis and septic shock, frequently alter the pharmacokinetics (PK) and pharmacodynamics (PD) of beta-lactam antibiotics. In pediatric critical care, these changes are further complicated by ongoing physiological growth and developmental changes in drug absorption, distribution, metabolism, and excretion. Although research in critically ill children has demonstrated that standard intravenous dosing regimens often fail to achieve target plasma concentrations, plasma levels alone do not necessarily reflect drug disposition at the actual site of infection. For extracellular pathogens, the target site of infection corresponds to the interstitial fluid (ISF) of tissues. Studies in adult septic populations suggest that subtherapeutic antibiotic concentrations in ISF may contribute to treatment failure, even when total plasma concentrations appear adequate. Data regarding antibiotic tissue disposition in pediatric intensive care unit (PICU) patients remain extremely limited. This monocentric, prospective, observational pharmacokinetic study utilizes in vivo microdialysis to directly quantify unbound tissue concentrations of three hydrophilic beta-lactam antibiotics-piperacillin-tazobactam, meropenem, and amoxicillin-clavulanic acid-in the ISF of skeletal muscle in critically ill pediatric patients.

The study will be conducted as follows:

  • Microdialysis Probe Insertion and Placement: Under continuous analgosedation, a 63 Microdialysis Catheter (M Dialysis AB, Solna, Sweden; 20 kDa molecular weight cut-off, 10 mm membrane length) is inserted into the vastus lateralis muscle of the anterolateral thigh using a steel guidance needle.
  • Perfusion and Calibration: The probe is continuously perfused with 0.9% physiological saline at a fixed flow rate via microinfusion precision pumps. After an equilibration period, in vivo probe recovery is determined using both retrodialysis and internal standard methods:
  • Retrodialysis: Performed prior to drug administration by perfusing the target antibiotic through the probe (2 x 30-minute intervals) to calculate relative recovery based on drug loss across the membrane.
  • Internal Standard Method: An internal calibrator (penicillin G for piperacillin-tazobactam and amoxicillin-clavulanic acid; cefuroxime for meropenem) is added to the perfusate solution to continuously monitor recovery throughout the experiment.
  • Biological Sampling: Following calibration, dialysate fractions are collected over designated time intervals across one or two antibiotic dosing cycles (representing early-dose and steady-state conditions). Paired blood samples are drawn concurrently from an existing intra-arterial or central venous catheter to quantify total plasma antibiotic levels. Unbound fractions in plasma are separated using ultrafiltration.
  • Analytical and Pharmacokinetic Modeling: Microdialysate and plasma drug concentrations are measured using high-performance liquid chromatography-mass spectrometry (HPLC-MS). Population pharmacokinetic modeling (non-linear mixed-effects modeling) and Monte Carlo simulations will be applied to derive PK parameters and evaluate PK/PD target attainment in the ISF in muscle.
Being tested
Pharmacokinetic sampling (Microdialysis and blood sampling)
Keywords
Microdialysis, Antibiotics, Beta-lactams, Pharmacokinetics, Pediatric Intensive Care, Tissue Penetration, Meropenem, Piperacillin, Tazobactam, Amoxicillin, Clavulanic Acid, Tissue Pharmacokinetics, Pediatrics
Medical subject headings
Critical Illness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pharmacokinetic sampling (Microdialysis and blood sampling)Other

    Intervention Description: Insertion of a 63 Microdialysis Catheter (M Dialysis AB; 20 kDa cutoff, 10 mm membrane) into the vastus lateralis muscle to measure unbound interstitial fluid antibiotic concentrations (calibrated using retrodialysis and an internal standard), combined with paired blood sampling via existing arterial/venous access to determine total and unbound plasma concentrations.

Study groups in NCT07822243
Study groupRoleWhat they receive
Critically Ill Pediatric CohortCritically ill pediatric patients (N=60 total) admitted to the Pediatric Intensive Care Unit (PICU) with continuous analgosedation who are prescribed routine intravenous therapy with one of three beta-lactam antibiotics (piperacillin-tazobactam, meropenem, or amoxicillin-clavulanic acid) as part of standard medical care. All participants undergo skeletal muscle microdialysis and paired blood sampling.
Receives: Other: Pharmacokinetic sampling (Microdialysis and blood sampling)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Tissue-to-plasma AUC ratio of beta-lactam antibiotics

    Ratio of the area under the concentration-time curve (AUC) of unbound beta-lactam antibiotic (piperacillin-tazobactam, meropenem, or amoxicillin-clavulanic acid) in skeletal muscle interstitial fluid (measured via microdialysis) to the AUC of total/unbound antibiotic in plasma. This evaluates the extent of tissue penetration.

    Measured: Up to 48 hours (measured over two separate dosing intervals)

Secondary outcomes (1)
  1. Pharmacokinetic/pharmacodynamic (PK/PD) target attainment in plasma and tissue

    Percentage of time during the dosing interval that unbound plasma and tissue antibiotic concentration remains above the Minimum Inhibitory Concentration (%fT>MIC) of the target micro-organism in interstitial fluid.

    Measured: Up to 48 hours (across sampled dosing intervals)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2026
  2. Study start1 Oct 2021
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

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
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07822243
Sponsor's protocol ID
BC-09534
Acronym
TACTIC
Status last verified
Sep 2026
First submitted
10 Sep 2026
Last updated
16 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Pediatric Critical Illness and Critical Illness, run by University Hospital, Ghent at 1 site in Belgium.

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 5 inclusion and 10 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: looking for participants now, as of the sponsor's last update on 16 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. 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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Pieter De Cock, Prof. (+32 9 332 29 69, pieter.decock@uzgent.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Tissue-to-plasma AUC ratio of beta-lactam antibiotics (time frame: Up to 48 hours (measured over two separate dosing intervals)). 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 16 Sep 2026.

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