- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00769262
Weaning Thermoregulatory Support in Preterm Neonates
Effect of Conservative Weaning of Thermoregulatory Support on Weight Gain and Length of Stay in Preterm Neonates
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
General Background:
There are three key milestones premature infants must meet prior to discharge from the NICU:
- The ability to maintain their temperature in an open crib
- The ability to consume enough calories for adequate growth by oral feeds
- A demonstrated weight gain consuming these feeds.
It is well understood that infants must increase their resting metabolic rate when weaned from the isolette to an open crib (1, 6). Preterm neonates have less metabolic reserve (brown fat) to allow them to mount an appropriate thermogenic response to cold stress (4). The reserve they do have is often depleted at delivery, leaving them with little or no reserve (4). When a neonate is challenged to maintain its body temperature, it must increase heat production which may affect weight gain (3). Some institutions wean without regard to neonate's weight or feeding status, while others only begin the weaning process at a predetermined weight. Currently neonates are weaned from their isolettes based largely on the traditions and experiences of clinicians, without regard to their feeding status. However, there is currently very little evidence in the literature to inform practice on the ideal conditions for weaning a neonate from their isolette. An extensive literature review has revealed no published data regarding the relationship of feed status to success at isolette weaning.
The transfer to open crib is important; if the neonate is not able to maintain his/her temperature, the length of stay could be lengthened and weight gain adversely affected (3). Cold stress can also cause adverse clinical effects including lethargy, hypotonia, poor feeding, abdominal distention, vomiting, pallor, tachypnea, and respiratory distress (2). These adverse clinical effects may also lengthen cost and length of stay, as well as adversely affect feeding. Furthermore, a return to the isolette can be quite stressful to parents and family members (3).
Subjects:
Approximately 110 subjects will be recruited. The subjects for this study will be live born preterm infants between 26 and 0/7 weeks gestation and 34 and 6/7 weeks gestation. Informed consent will be obtained from the parents.
Methods:
Neonates will be randomly assigned to either the control group (with standard thermoregulatory weaning protocol) vs. experimental group (with conservative thermoregulatory weaning protocol). After an infant is enrolled in the study, an envelope indicating random assignment to either the aggressive or conservative group will be drawn and the infant will be assigned to the indicated study group. The envelopes will be provided by the statistician and will be delivered in groups of 10 to ensure relatively equal numbers of babies in both study groups.
All infants will be advanced to goal caloric feeds of 120 Kcal/kg. Weight gain will be measured biweekly, and if adequate weight gain (average 20 grams/kg/day) is not reached, feeds will be advanced by 10 Kcal/kg/day biweekly until adequate weight gain is reached.
All infants will be kept on skin control mode until they weigh 1500 grams. Babies on skin control mode will be unclothed except for a diaper. Once infants reach 1500 grams, they will be placed on air control mode. Babies on air control mode will be dressed in one medium-weight sleeper with feet (or with socks if sleeper is footless), one hat, and no blankets or other clothing.
Control Group: Aggressive Wean
Weaning Process:
- If baby's temperature is greater than or equal to 36.7°C on 2 consecutive measurements 3 hours apart, the isolette set temperature will be lowered by 0.2°C.
- If baby's temperature is less than 36.3°C on 1 measurement, the isolette set temperature will be increased by 0.2°C.
- Once the baby's temperature is stable at greater than 36.7°C for 3 consecutive measurements 3 hours apart on an isolette set temp of 28.0°C, the baby will be transferred to an open crib. At this time, the baby will be dressed in one medium-weight sleeper with feet (or with socks if sleeper is footless), one hat, and a sleep sack. NO heavy blankets (such as bath blankets) or extra blankets are to be used.
- If the baby's temperature is less than 36.3°C on 1 measurement, they will be transferred back to the isolette and the weaning process will begin again.
Experimental Group: Conservative Wean
Weaning Process:
- If baby's temperature is greater than or equal to 37.2°C on 2 consecutive measurements 3 hours apart, the isolette set temperature will be lowered by 0.2°C.
- If baby's temperature is less than 36.3°C on 1 measurement, the isolette set temperature will be increased by 0.2°C.
- Once the baby's temperature is stable at greater than 37.2°C for 3 consecutive measurements 3 hours apart on an isolette set temp of 28.0°C, AND the baby is taking full caloric need feeds (at least 120 Kcal/kg/day), AND the baby is taking half of its feeds by mouth the baby will be transferred to an open crib. At this time, the baby will be dressed in one medium-weight sleeper with feet (or with socks if sleeper is footless), one hat, and a sleep sack. NO heavy blankets (such as bath blankets) or extra blankets are to be used.
- If the baby's temperature is stable at greater than 37.2°C for 4 consecutive measurements 3 hours apart on an isolette set temp of 28.0°C, or if the baby's temperature is greater than 37.9°C on an isolette set temp of 28.0°C, the baby will be transferred to an open crib regardless of feeding status. At this time, the baby will be dressed in one medium-weight sleeper with feet (or with socks if sleeper is footless), one hat, and a sleep sack. NO heavy blankets (such as bath blankets) or extra blankets are to be used.
- If the baby's temperature is less than 36.3 degrees Celsius on 1 measurement, they will be transferred back to the isolette and the weaning process will begin again.
Research Significance and Future Research:
This study will provide data regarding the weaning of thermoregulatory support in preterm infants, and could have significant economic impact for the university if there is a significant difference in length of stay between the study groups. Future research will focus on long-term effects on outcomes such as nutritional status in infancy and BMI in childhood if neonates do require greater caloric intake if they are weaned from thermoregulatory support faster.
Bibliography:
- Dollberg S, Mimouni FB, Weintraub V. (2004) Energy expenditure in infants weaned from a convective incubator. American Journal of Perinatology. 21(5):253-6
- Hackman P. (2001) Recognizing and understanding the cold-stressed term infant. The Journal of Neonatal Nursing. 20(8):35-41
- New K, Flenady V, Davies MW. (2007) Transfer of preterm infants from incubator to open cot at lower versus higher body weight. The Cochrane Database of Systematic Reviews. 4.
- Sherman TI, Greenspan JS, St. Clair N, Touch S, Shaffer T. (2006) Optimizing the neonatal thermal environment. Neonatal Network; The Journal of Neonatal Nursing. 25(4):251-60
- Short MA. (1998) A comparison of temperature in VLBW infants swaddled versus unswaddled in a double-walled incubator in skin control mode. Neonatal Network; The Journal of Neonatal Nursing. 17(3):25-31
- Weintraub V, Mimouni FB, Dollberg S. (2007) Changes in energy expenditure in preterm infants during weaning: A randomized comparison of two weaning methods from an incubator. Pediatric Research. 61(3):341-4
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Missouri
-
Columbia, Missouri, United States, 65201
- Columbia Regional Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Live born preterm infants from 26 and 0/7 weeks gestation to 34 and 6/7 weeks gestation
- Require thermoregulatory support
- Are able to take feeds
- Are presumed to be able to take oral feeds in the future
Exclusion Criteria:
- Preterm infants less than 26 and 0/7 weeks gestation
- Preterm infants greater than 34 and 6/7 weeks gestation
- Infants that do not require thermoregulatory support
- Infants that will not be able to have enteral feeds
- Infants with endocrine disease
- Infants with congenital anomalies
- Infants with grade 3 or 4 intraventricular hemorrhage or other severe neurologic disability
- Infants requiring long-term sedation
- Infants that die within 7 days of birth
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: Aggressive Weaning
Infants will be weaned from the isolette using our current NICU standard of care.
|
Infants will be weaned from the isolette based solely on their temperature without regard to feed status (current standard of care in our NICU)
|
EXPERIMENTAL: Conservative Weaning
Infants will be weaned from the isolette using a modified conservative weaning schedule.
|
Infants will not be weaned from the isolette until their feeds are at full calorie goal (120 kcal/kg/day) and at least half of feeds are taken orally.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Length of hospital stay
Time Frame: Hospital discharge
|
Hospital discharge
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Weight gain
Time Frame: When patient is on 120 cal/kg/day dietary intake
|
When patient is on 120 cal/kg/day dietary intake
|
Caloric requirement
Time Frame: When patient is changed to oral ad lib demand feeds
|
When patient is changed to oral ad lib demand feeds
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sarah B Patton, MD, University of Missouri-Columbia
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1105137
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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