Innovative Approaches to Assessment of Pain Control and Sedation in the NICU
Studie Overzicht
Toestand
Conditie
Gedetailleerde beschrijving
This is a prospective, non-interventional study designed to assess noxious-specific neurophysiologic responses and clinical signs following procedural pain in infants requiring hospitalization in the neonatal intensive care unit (NICU) following elective surgery.
The main goal of the study is to develop a method that reliably quantifies the level of pain induced from clinically-required noxious procedures to infants hospitalized in the NICU. This method will use measures of neurophysiological, autonomic, and behavioral responses to non-noxious and clinically-required noxious stimuli in order to guide the pharmacological treatment of NICU patients with analgesic agents, sedatives and/or muscle relaxants.
The investigators hypothesize that resting state activity and physiological responses to noxious and non-noxious stimuli provide a more reliable assessment of the level of pain of infants hospitalized in the NICU compared to behavioral-based pain scores.
Studietype
Inschrijving (Verwacht)
Contacten en locaties
Studie Locaties
-
-
Massachusetts
-
Boston, Massachusetts, Verenigde Staten, 02115
- Boston Children's Hospital
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
Beschrijving
Inclusion Criteria:
- All patients will be admitted to the NICU, and having a post-menstrual age of >28 weeks. Participants will be divided into four groups according to the following criteria:
Group A
- Plan for major surgery anticipated to cause pain and agitation (i.e. esophageal atresia treatment);
- Patients who are anticipated to receive prolonged post-surgical neuromuscular blockade
Group B
- Plan for major surgery anticipated to cause pain and agitation (i.e. bowel surgery);
- Patients who are not anticipated to receive acute post-surgical neuromuscular blockade
Group C Plan for minor surgery anticipated to cause pain and agitation (i.e. hernia repair);
Group D No plan for surgery
Exclusion Criteria:
- Confirmed or suspected clinical seizures
- Metabolic abnormalities or inborn error of metabolism
- Skin abrasions or wounds located at the site of research sensor placement i.e. scalp, which interfere with the application of electrodes
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Observatiemodellen: Cohort
- Tijdsperspectieven: Prospectief
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
|---|---|
|
Group A
The following devices will be used in this Group: Waveguard (TM) EEG cap; Micro Movement Sensor; Pico Movement Sensor; QS Piezostimulator; tactileTM sensory evaluator. These subjects will also receive EMG monitoring. Subjects in this group will also have video recordings that may be used for novel analysis such as subdermal blood flow or micro-movement. |
The device is an EEG cap - a non-invasive EEG positioning system used to quickly place a large number of surface electrodes in a quick and consistent manner on the head.
The device will measure electrophysiological signals from the scalp at the time points in the study listed in the protocol.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor breathing and movement in children; the device is not used for validation purposes.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor respiration rate and gross body movement in children.
The device will not be used for validation purposes.
This device is not FDA approved.
This device is used for research purposes by neurologists and physiologists.
It is a mechanical tactile stimulator for use in functional imaging experiments like MEG, fMRI or EEG.
The stimulation is realized by using several different pin matrices.
In this study, the device is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
This device is not FDA approved.
This device is used for clinical and research purposes by neurologists and physiologists.
It is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
|
|
Group B
The following devices will be used in this Group: Waveguard (TM) EEG cap; Micro Movement Sensor; Pico Movement Sensor; QS Piezostimulator; tactileTM sensory evaluator. Subjects in this group will also have video recordings that may be used for novel analysis such as sub-dermal blood flow or micro-movement. |
The device is an EEG cap - a non-invasive EEG positioning system used to quickly place a large number of surface electrodes in a quick and consistent manner on the head.
The device will measure electrophysiological signals from the scalp at the time points in the study listed in the protocol.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor breathing and movement in children; the device is not used for validation purposes.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor respiration rate and gross body movement in children.
The device will not be used for validation purposes.
This device is not FDA approved.
This device is used for research purposes by neurologists and physiologists.
It is a mechanical tactile stimulator for use in functional imaging experiments like MEG, fMRI or EEG.
The stimulation is realized by using several different pin matrices.
In this study, the device is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
This device is not FDA approved.
This device is used for clinical and research purposes by neurologists and physiologists.
It is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
|
|
Group C
Plan for minor surgery anticipated to cause pain and agitation (i.e. hernia repair) The following devices will be used in this Group: Waveguard (TM) EEG cap; Micro Movement Sensor; Pico Movement Sensor; QS Piezostimulator; tactileTM sensory evaluator. Subjects in this group will also have video recordings that may be used for novel analysis such as sub-dermal blood flow or micro-movement. |
The device is an EEG cap - a non-invasive EEG positioning system used to quickly place a large number of surface electrodes in a quick and consistent manner on the head.
The device will measure electrophysiological signals from the scalp at the time points in the study listed in the protocol.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor breathing and movement in children; the device is not used for validation purposes.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor respiration rate and gross body movement in children.
The device will not be used for validation purposes.
This device is not FDA approved.
This device is used for research purposes by neurologists and physiologists.
It is a mechanical tactile stimulator for use in functional imaging experiments like MEG, fMRI or EEG.
The stimulation is realized by using several different pin matrices.
In this study, the device is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
This device is not FDA approved.
This device is used for clinical and research purposes by neurologists and physiologists.
It is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
|
|
Group D
No plan for surgery The following devices will be used in this Group: Waveguard (TM) EEG cap; Micro Movement Sensor; Pico Movement Sensor; QS Piezostimulator; tactileTM sensory evaluator. Subjects in this group will also have video recordings that may be used for novel analysis such as sub-dermal blood flow or micro-movement. |
The device is an EEG cap - a non-invasive EEG positioning system used to quickly place a large number of surface electrodes in a quick and consistent manner on the head.
The device will measure electrophysiological signals from the scalp at the time points in the study listed in the protocol.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor breathing and movement in children; the device is not used for validation purposes.
This device is not FDA approved.
This device is in clinical use for all age groups and used for research purposes by neurologists, physiologists and anesthesiologists.
In this study, the device is used to monitor respiration rate and gross body movement in children.
The device will not be used for validation purposes.
This device is not FDA approved.
This device is used for research purposes by neurologists and physiologists.
It is a mechanical tactile stimulator for use in functional imaging experiments like MEG, fMRI or EEG.
The stimulation is realized by using several different pin matrices.
In this study, the device is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
This device is not FDA approved.
This device is used for clinical and research purposes by neurologists and physiologists.
It is used to stimulate the children's extremities in order to elicit somatosensory evoked responses.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Noxious Stimuli Results
Tijdsspanne: Up to 1 year
|
To assess pain-specific brain activity and autonomic responses post surgery in response to an acute noxious procedure in newborn infants admitted to the NICU. This outcome will be correlated with current behavioral and physiological based pain assessment tools as follows: Procedural-specific brain activity in infants with varying conditions with pre or post-operative pain. EEG: amplitude of noxious-event related potential evoked by a time-locked noxious stimulus. Pain-specific electro-dermal activity (EDA), electromyography (EMG) and subdermal skin flow; Pain-evoked behavioral measures including: Body movement; Eye squeeze, brow bulge and nasolabial furrow duration. Pain-evoked physiological measures including: Respiration rate; Heart rate; Blood pressure; Oxygen saturation; Observational pain scores (PIPP); EMG activity. |
Up to 1 year
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Resting State Results
Tijdsspanne: Up to 1 year
|
Characterize resting state activity in post-operative or control subjects as follows: Baseline brain (EEG) activity (power spectra of baseline EEG signal) in post operative or control subjects. Baseline EDA, EMG and subdermal skin flow; Baseline behavioral measures including: Presence of body movement, eye squeeze, brow bulge and nasolabial furrow. Baseline physiological measures including: Respiration rate; Heart rate; Blood pressure; Oxygen saturation; Observational pain scores (PIPP). The relationship with resting brain activity, electrodermal activity, behavior, physiological, and observational pain scores will be evaluated. |
Up to 1 year
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Laura Cornelissen, PhD, Boston Children's Hospital
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- IRB-P00022180
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .