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Tympanic Thermometer Study

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Baxter

Status

Active, not recruiting

Conditions

Fever
Body Temperature Changes

Treatments

Device: Increased Body Temperatures

Study type

Observational

Funder types

Industry

Identifiers

NCT06556628
60117201

Details and patient eligibility

About

The goal of this study is to collect febrile, healthy, and in some instances cold temperature data from human subjects ranging from newborns to geriatrics. This data will be used to develop a new thermometer.

Enrollment

1,000 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: normal weight (≥2.5kg), full-term (37 weeks gestation) newborn to geriatric adult.
  • Participant, legal guardian, or healthcare proxy is able to give consent to participate.
  • Participant, legal guardian, or healthcare proxy speaks fluent English.

Exclusion criteria

  • The subject does not meet the inclusion criteria.
  • The subject has anatomical abnormalities that would affect temperature.
  • The subject has blood or drainage in the external ear canal.
  • The subject has had something in their ear for a prolonged period, such as a hearing aid or headphones. The subject may be included if the hearing aid or headphones are removed at least 30 minutes prior to taking ear temperature.
  • The subject has been lying on ear within 30 minutes of data collection. The subject may be included if they wait 30 minutes prior to having an ear temperature measurement taken.
  • The subject exhibits symptoms of an acute or chronic inflammatory condition of the external ear canal. An example would be swimmer's ear. The subject may be included if the acute or chronic inflammatory condition is isolated to one ear, then the other ear may be used for data collection.
  • The subject has an ear obstruction or excess cerumen build-up.
  • The subject is in acute distress, i.e., severe pain, severe emotional distress or agitation that would inhibit them from participating in a tympanic ear temperature study.
  • The subject has any known contraindication to oral, ear, or axillary temperature measurements.
  • The subject has used ear drops in the last 8 hours. The subject may be included if the other ear was not medicated with ear drops in the last 8 hours.
  • The subject (age 5+) has consumed food or drink, or smoked, within the last 20 minutes. The subject may be included if they wait 20 minutes prior to taking oral temperature.
  • The subject has taken an antipyretic (ex: Tylenol, Motrin, Aspirin) in the last 120 minutes.

Trial design

1,000 participants in 3 patient groups

Fever
Description:
Elevated oral temperature of 37.5C or higher or elevated axillary temperature of 37.2C or higher.
Treatment:
Device: Increased Body Temperatures
Healthy
Description:
Oral temperature between 36-37.4C Axillary temperature between 36-37.1C
Cold
Description:
Oral or axillary temperatures below 36C

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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