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Recruiting NCT06447337

Continuos Body Temperature Monitoring

Observational Fever

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Continous body temperature monitoring.
Who it may be relevant to
Registry conditions: Fever. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Serbia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Examination of a Telemedicine System for Continuous Monitoring of Body Temperature in Adults - a Pilot Study

Overview

This is a nonrandomized, diagnostic, single-center, pilot study, with one group of participants. The aim is to examine the effectiveness and safety of telemedicine system for continuous measurement of body temperature in adults. Up to 40 subjects will participate in this phase of the clinical trial. No stratification, nor randomization of subjects will be performed. Respondents who meet the inclusion criteria will be monitored for up to 72 hours plus 72 hours after removing the device. Namely, the device will be placed on their body and will be there until upt to 72 hours, and then it will be removed. The respondent will be monitored by the team for an additional 72 hours by the person in charge of the examination, for possible side effects. Sensor will be placed in the axilar joint or a little below on the side. The device will be connected to a mobile phone. Member of the research team (principal researcher/co-researcher/ nurse in charge of examination) measures the temperature of the skin in the opposite armpit manually, ie with a gallium thermometer and records every 30-60 minutes. When body temperature starts to rise, a member of the research team measures the body temperature every 15-30 minutes. After reaching a stable temperature, the temperature is measured every 30-60 minutes. If the subject is given drugs to lower body temperature, the temperature is measured again every 15-30 minutes until the temperature stabilizes to a normal subfebrile state.

Interventions

  • Diagnostic test Continous body temperature monitoring
    The investigational product will be placed on the participants' body in axilar joint and connected to the mobile phone. The values of the current temperature will apear on the monitor and it will be recorded in the database with date and time for each record. In parallel, study staff will occasionally measure the temperature using standard hospital thermometer.

Primary outcome measures

  • Correlation between device for continous body temperature monitoring and standard thermometer [Time frame: up to 72 hours]
Secondary outcome measures (1)
  • Frequency of device and procedure related adverse events [Time frame: up to six days]

Eligibility criteria

Inclusion criteria

  • A person of male or female sex
  • Age 18 and over
  • Ability to measure the patient's body temperature frequently
  • People who are hospitalized due to any type of infection or any other diseases that result in variations in body temperature (rise, fall)
  • Completed all potential diagnostics of the hospitalized patient (no interrupting the measurement of the telemedicine device)

Exclusion criteria

  • Allergic to contact with plastic or silver
  • Anatomical anomalies that prevent the placement of the system
  • High-risk health conditions, intensive care and the like
  • A pacemaker or other device on the skin or implanted in the body that emits light electromagnetic radiation

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

Serbia · 1 center
  • University Clinical Center of Serbia, Clinic for Infectious and Tropical Diseases — Belgrade

Identifiers

NCT: NCT06447337 · BABYFM-010

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗