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NCT Number: NCT07779915

MICropsampling for CAffeine in PREMature Newborns

Caffeine is one of the top five most prescribed drugs in neonatology. Caffeine has many beneficial impacts on preterm infants (cardiac, neurologic and pulmonary). One of these beneficial impacts is to prevent apnea. However, despite its use in routine neonatal practice, there is currently no consensus on standardized protocols for caffeine administration concerning timing and dose and there is a lack of knowledge in the most immature preterm. High caffeine concentrations may lead to serious adverse events such tachycardia while low caffeine concentrations may lead to an upsurge apnea, and as a consequence to the necessity of mechanical ventilation.

A study demonstrated that highly variable caffeine concentrations where observed when a standardized dose was administered to preterm infants. However, while no correlation between caffeine concentration and the number of apneas has been reported, there is a correlation between caffeine concentration and heart rate in preterm infants. In addition, a retrospective study demonstrated that in infants born before 29 gestational weeks with a caffeine concentration > 15 micrograms/ml was associated with a lower incidence of chronic lung disease, persistent ductus arteriosus, lesser number of days of ventilation and shorter length of stay in hospital. Based on these observations, therapeutic drug monitoring (TDM) of caffeine could be particularly relevant in preterm infants, in order to manage the risk of overexposure to caffeine in patients who need higher doses to prevent apnea. However, we are limited by the risk of anemia associated with repeated sampling in preterm infants. In our hospital, Caffeine is measured when children make apnea despite a dosage of 5 mg/kg and when children have potentials adverse events such tachycardia.

To avoid anemia due to repeated blood test for TDM, microsampling devices allowing analyses in very small volumes of blood could be used. Recently, microsampling devices have been developed for home-based capillary blood sampling and their use has been validated in different contexts, in particular the TDM of immunosuppressive drugs. These devices allow the collection of dried blood spots and present the advantages of being less invasive than venipuncture and collecting low volumes of blood for analysis. The analysis of caffeine in dried blood spot (DBS) has been developed with a good agreement between DBS and plasma concentrations in neonates. However, changes in hematocrit levels may impact concentrations measured in DBS. To avoid this, volumetric micro sampling (VAMS) devices such as the Mitra ® (Neoteryx®) have been developed with good results. With caffeine, VAMS effectively assisted in eliminating the effect of hematocrit and have good correlation with blood standard dosage.

In this context, the investigator propose a pilot study in preterm infants, in whom the microsampling device Mitra ® will be used for capillary blood sampling to collect caffeine for TDM. The (i) feasibility (ii) nurse satisfaction iii) analytical performances will be evaluated.

The hypothesis is that the use of a microsampling device such as Mitra ® will render possible caffeine TDM thanks to a good feasibility and to good pre-analytical and analytical performances of a method developed.

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Key information

Age range

24 week–34 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Brive Hospital, Brivé, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Preterm infants born before 34 amenorrhea weeks
  • Receiving oral or intravenous Caffeine
  • Requiring capillary blood sample
  • Having parental signed informed consent of participation in the study
  • Affiliated to, or beneficiary of, a social security program

Exclusion criteria

  • Birth Weight under 500 grams
  • Age under 24 weeks of amenorrhea.

Treatment and study plan

collection of an extra drop of capillary blood

Diagnostic Test

an extra drop of capillary blood will be collected with the Mitra® at the time of capillary blood sampling performed by the nurses for their care.

Caffein is dosed with this capillary blood sampling of 50 microliters but the pediatrician will only have the result of the routine test to adapt caffein treatment

Primary outcomes

  1. Feasibility of the integration of use of Mitra® in the therapeutic drug monitoring of caffeine in premature newborns

    Time frame: at the enrollement

    The feasibility of using the Mitra® device will be assessed based on the compliance rate. Two types of noncompliance will be considered:

    • pre-analytical noncompliance: insufficient or excessive saturation
    • analytical noncompliance: noncompliant quality controls that prevent the generation of a reliable test result in accordance with the laboratory's standard operating procedures.

Secondary outcomes

  1. Nurses' satisfaction rating based on a questionnaire

    Time frame: at the enrollment

  2. Caffeine concentration in samples collected using Mitra ® vs. standard blood test for TDM in preterm infants

    Time frame: at the enrollment

Study contacts

Contact information is provided by the study sponsor or research team.

Laure PONTHIER, MD

CONTACT

[email protected]

0555058666

Sponsors and collaborators

Lead sponsor

University Hospital, Limoges

Other

Registry information

Official study title

Use of a Microsampling Kit for the Therapeutic Drug Monitoring (TDM) of Caffeine in Premature Newborns

Acronym: MICCAPREM

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 21, 2026
Registry last updated
Aug 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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