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Body Temperature clinical trials

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NCT ID: NCT06275932 Not yet recruiting - Body Temperature Clinical Trials

Management of Healthy Newborn's Body Temperature at Birth

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

At birth, the newborn begins a process of adaptation to extrauterine life. One of the phases of this stabilization process is the maintenance of body temperature; indeed, the newborn passes from a warm environment (mother's womb) of around 37°C to an environment with a temperature lower (delivery room) and, therefore, must implement a series of physiological processes to be able to maintain body temperature constant and within ideal ranges through a balance between production and heat loss. Hypothermia at birth could cause risks or comorbidities such as an increased risk of infant mortality, hypoglycemia, sepsis, metabolic acidosis, respiratory distress syndrome (RDS) and intraventricular hemorrhage (IVH). One of the factors that affects heat loss in the delivery room is the relationship between surface area, volume and body mass of the newborn. The decrease in body temperature is directly related to gestational age and weight at birth; indeed, this problem is much more present in premature and/or low weight newborns at birth. Even if a full-term newborn has a more developed thermoregulation center than a preterm newborn, this does not mean that this type of newborns is not at risk heat dispersion. To date, the strategies that are implemented for the physiological newborn are documented in the literature are, in addition to the heat chain described by the World Health Organization (WHO), the implementation of skin-to-skin contact (skin to skin) mother-newborn. Some studies demonstrating the beneficial effect of this procedure on maintenance of the newborn's body temperature. The aim of this study is to evaluate two healthcare interventions to prevent heat loss of healthy newborns at birth.

NCT ID: NCT06044428 Recruiting - Pneumonia Clinical Trials

Steadysense -Early Detection of Postoperative Infections Through Continuous Temperature Measurement

Start date: August 14, 2023
Phase:
Study type: Observational

The goal of this observational study is to review whether postoperative infections can be detected earlier by a continuous measurement of body temperature of patients compared to single daily measurements. Within 25 weeks 100 patients, which underwent visceral surgery less than 48h ago, will be included. A patch (Steadytemp ®) will be attached to participants, continuously measuring the body temperature. In addition infection parameters and medication of the participants will be documented.

NCT ID: NCT05042349 Withdrawn - Physical Activity Clinical Trials

Pregnant Elite Athletes and Pregnant Women Exercising With Moderate Intensity

Start date: June 1, 2020
Phase:
Study type: Observational

The aim of this study is to 1. register possible changes to uteroplacental circulation in relation to physical tests, 2. to register energy and nutritional intake, relationship towards the body during pregnancy and during the early period after giving birth, 3. register the experience of guidance given related to exercise, nutrition, and recovery, 4. register elite athletes' experience of combining the role of being a mom and an elite athlete, and 5. register attitudes and reactions from the support system when it comes to being an elite athlete and being pregnant. Material and method: 30 pregnant female elite athletes and 30 moderately physically active pregnant women will be recruited for the completion of physical testing and questionnaires and questionnaires only, respectively. 20 national team leaders/coaches and 10 sponsors will be recruited for a semi-structured interview about attitudes, reactions and guidance towards athletes who become pregnant and still wish to continue their career as an athlete after pregnancy.

NCT ID: NCT05022264 Recruiting - Blood Pressure Clinical Trials

Remote Investigation and Assessment of Vital Signs

RIA-VS
Start date: March 1, 2022
Phase:
Study type: Observational

The vital signs (pulse, systolic and diastolic blood pressure, respiratory rate, oxygen saturation and body temperature) are critical in assessing the severity and prognosis of infections. The devices used today for measuring the vital signs have to be in physical contact with the patients. There is an apparent risk of transferring infections from one patient to the next (or to healthcare professionals). Accurately obtaining vital signs is also important when managing other categories of patients where it may be relevant to obtain some of the vital signs such as pulse and blood pressure. This project aims to evaluate a new camera-based system for contactless measurement of vital signs.

NCT ID: NCT04346498 Completed - Heart Rate Clinical Trials

Can Kangarooing Small Babies on the Back of a Mother Keep Them Warm and Stable

Start date: January 3, 2017
Phase: N/A
Study type: Interventional

The purpose of this study was to assess the effectiveness of Kangarooing small babies on the back of a mother

NCT ID: NCT04211701 Recruiting - Body Temperature Clinical Trials

Effects of Connective Tissue Massage and Classical Massage

Start date: October 22, 2019
Phase: N/A
Study type: Interventional

As a randomized study, this study aimed to investigate the effects of classical massage and connective tissue massage on pain, flexibility, disability, quality of life and autonomic responses in patients with chronic mechanical low back pain. The primary evaluation parameter of the study is autonomic function and the secondary evaluation parameter is pain. The participants will be treated accompanied with same physiotherapist along four weeks and five days in a week. A six-week follow-up will be performed to see how long the effect of the treatment continues.

NCT ID: NCT03990116 Recruiting - Premature Infant Clinical Trials

Efficacy of Lateral Kangaroo Care in Hemodynamic Stabilization of Premature Infant.

Cangulat
Start date: May 10, 2019
Phase: N/A
Study type: Interventional

The objetive of the study is to evaluate the non-inferiority or the equivalence of the kangaroo care position, in lateral versus traditional one in prone measuring the stability of several parameters in premature infants less than 28 weeks of gestational age during the first 5 days of life.

NCT ID: NCT03920943 Withdrawn - Body Temperature Clinical Trials

Temporal Artery Thermometer in Patient Transport: Reliability and Validity.

TAT
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

Evaluate the reliability and validity of temperature measurements using an existing, Health Canada-approved, non-invasive temporal artery thermometer, and comparing results to an established, invasive gold standard (esophageal probe), in order to assess reliability of this non-invasive method to measure core body temperature in the setting of patients undergoing inter-facility patient transport by land, rotor-wing, and fixed-wing transport vehicles.

NCT ID: NCT03919188 Recruiting - Preterm Infant Clinical Trials

Air vs. Cutaneous Control Mode for Preterm Infants ≤ 32 WG in Incubators: Impact on Body Growth and Morbidity

ThermoKPreterm
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Previous studies have shown that mortality and morbidity in preterm neonates are correlated with the fall in body temperature on admission. Hypothermia can be decreased by reducing body heat losses to the environment. The investigator research hypothesis is that a new calculation of the air temperature in the incubator would promote the newborn infant weight growth from the period between birth and day 10 of life compared to cutaneous mode. The secondary hypotheses assumes a decrease in the side effects usually observed in both morbidity and mortality. A software is used to calculate the body heat loss (BHL) of each individual preterm infant, and to propose a specific air temperature setting inside the incubator to reduce BHL to zero. This software has been validated in a previous pilot study (Degorre et al. 2015). This study aims to compare the energy costs of providing incubated preterm infants born between 25 and 32 weeks of gestation with homeothermia using either specific individualized air temperature control (ATC) or skin servocontrol (SSC).

NCT ID: NCT03206528 Recruiting - Oxygen Saturation Clinical Trials

Clinical Evaluation of the Vital Signs Monitoring System (VSMS)

Start date: April 25, 2017
Phase: N/A
Study type: Observational

This is an observational, cohort-based, single-site, prospective study conducted in accordance with ISO 14155-1:2003 and ISO 14155-1:2011. The primary objectives are to evaluate the accuracy of the device's measurements/readings in comparison to a gold standard or standard of care patient monitor.