HealthyNCT02325284
Objective Measurement of Pain Using the Algometer
An observational study of Healthy, run by Julia Finkel at 1 site in United States.
Trial summary
The development of tools for assessment and management of pain in newborns and children is a high priority and represents a significant unmet need. The inadequate treatment of pain and the overuse of analgesics can cause harmful consequences for neonates, infants, and children. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Healthy
- What is being tested?
- Pressure Algometer Testing
- Type of treatment
- Medical device
- How many people
- 20 participants
- Where
- 1 siteUnited States
- Study dates
- Sep 2014to Dec 2016
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Healthy adults.
Who may be able to join
- the subject 18-65 years of age.
- the subject is a healthy adult with significant ongoing medical conditions
- the subject is willing to remain at the research site for the duration of the study session.
- the subject is willing and able to provide written informed consent to study participation.
Who cannot join
- the subject has consumed alcohol within the last 12 hours prior to testing
- subject has pain at the time of testing anywhere in the body
Trial locations and contacts
1 site in 1 country.
United States1 site
Children's National Medical Center
Washington D.C., District of Columbia, 20010
About this study
Official title: Phase 1 Pilot Study of an Apparatus and Method to Objectively Measure Pain in Normal Healthy Adults.
The development of tools for assessment and management of pain in newborns and children is a high priority and represents a significant unmet need. The inadequate treatment of pain and the overuse of analgesics can cause harmful consequences for neonates, infants, and children. To accomplish successful pain management in children one must first objectively assess pain. Thus, to address these critical issues with pain management, the Human Algometer and methods are under development by Drs. Julia Finkel and Zena Quezado, Pain Medicine Program (SZI) at Children's National Medical Center.
Read the detailed description
It is generally recognized that pain assessment and management in newborns and children is an unmet need. According to the American Medical Association, "The pediatric population is at risk of inadequate pain management, with age-related factors affecting pain management in children. Children are often given minimal or no analgesia for procedures that would routinely be treated aggressively in adults. Although much is now known about pain management in children, it has not been widely or effectively translated into routine clinical practice."1 Although some clinically validated methods exist (e.g. CRIES, PPIP, Faces, etc.), no "gold standard" of pain assessment has been adopted in clinical practice. All are hindered by ambiguous behavioral correlates to the pain stimuli standards as well as the subjective variability inherent in both clinical and parent evaluators 2.
Other apparatus/methods for pain assessment suffer from similar shortcomings. For example, pain tolerance threshold (PTT) and current perception threshold (CPT) determinations both rely on verbal response from a patient. Those determinations are subjective and semi-quantitative and use electrical stimulation to directly excite both large and small diameter sensory nerve fibers. The CPT determination represents the minimum amount of a potentially noxious electrical stimulus that can be perceived, while the PTT determination represents the maximum amount of noxious electrical stimulation that can be tolerated when used as a clinical diagnostic tool. Thus, PTT depends on a subject's verbal response and requires patient exposure to aversive electrical stimulation, which causes both undesirable discomfort but also elicits the affective component of pain.
Therefore, the development of tools for assessment and management of pain in newborns and children is a high priority and represents a significant unmet medical need. Both inadequately treated pain or over administration of analgesics can have deleterious physiologic consequences for neonates, infants and children. While a number of methods are in use, no "gold standard" for pain assessment exists. (Anand 2007) To accomplish meaningful pain management in children one must first be able to objectively assess pain, particularly in patients who are (1) non-verbal (e.g. neonates, infants), (2) lacking understanding and adequate verbalization skills (e.g. young children, developmentally disabled individuals) and (3) patients with compromising neuropathic clinical presentations. To address these critical issues with pain management, the Human Algometer and method are under development by Drs. Finkel and Quezado from the Pain Medicine Program at the Sheikh Zayed Institute. In brief, this device integrates a neurospecific neurostimulation of sensory nerve fibers involved in pain response and near infra-red spectroscopy (NIRS) signal acquisition derived from pain related hemodynamic changes in the somatosensory cortex. The device has the ability to collect data on the NIRS response in the cerebral cortex to noxious stimulation provided by the neurostimulation component. Signal processing of data from this trial and subsequent trials will result in (1) the detection and optimization of a NIRS signal specific to increased neuronal blood flow over the somatosensory cortex (nociceptive response) and the frontal cortex (affective component). The individual neurostimulatory and NIRS signal acquisition components integrated into this novel device are based in part or whole on previously FDA approved devices from Neurotron, Inc. and Covidien plc (former Somanetics INVOS ™) respectively.
- Conditions
- Healthy
- Being tested
- Pressure Algometer Testing
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pressure Algometer TestingDevice
Also called Wagner FPIX 50™ digital pressure algometer.
| Study group | Role | What they receive |
|---|---|---|
| Healthy adults | Not described Receives: Device: Pressure Algometer Testing |
What is being measured
The primary outcome is the main question the study is designed to answer.
Collection of data for signal processing that will generate the algorithms and data filters required to establish proof of concept for the novel technology.
The data collected and process from the human algometer will generate a specific NIRS nociceptive response to neurostimulation in the somatosensory cortex.
Measured: one year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Dec 2014 (estimated)
- Study startSep 2014
- Primary completionSep 2016
- Study completionDec 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HealthyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- Julia Finkel
- Sponsor type
- University, hospital or other
- Collaborators
- CoolCad Electronics, LLC; University of Maryland Engineering
- Responsible party
- Sponsor-investigator, Julia Finkel, Children's National Research Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02325284
- Sponsor's protocol ID
- Algometer/Phase 1 pilot study
- Status last verified
- Apr 2017
- First submitted
- 19 Dec 2014
- Last updated
- 12 Apr 2017
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 12 Apr 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase 1 Pilot Study of an Apparatus and Method to Objectively Measure Pain in Normal Healthy Adults.
- ClinicalTrials.gov ID
- NCT02325284
- Acronym / sponsor ID
- Algometer/Phase 1 pilot study
- Conditions
- Healthy
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Julia FinkelUniversity, hospital or other
- Collaborators
- CoolCad Electronics, LLC; University of Maryland Engineering
- Study start
- Sep 2014
- Primary completion
- Sep 2016 (actual)
- Study completion
- Dec 2016 (actual)
- First posted
- 24 Dec 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The development of tools for assessment and management of pain in newborns and children is a high priority and represents a significant unmet need. The inadequate treatment of pain and the overuse of analgesics can cause harmful consequences for neonates, infants, and children. To accomplish successful pain management in children one must first objectively assess pain. Thus, to address these critical issues with pain management, the Human Algometer and methods are under development by Drs. Julia Finkel and Zena Quezado, Pain Medicine Program (SZI) at Children's National Medical Center.
Detailed description
It is generally recognized that pain assessment and management in newborns and children is an unmet need. According to the American Medical Association, "The pediatric population is at risk of inadequate pain management, with age-related factors affecting pain management in children. Children are often given minimal or no analgesia for procedures that would routinely be treated aggressively in adults. Although much is now known about pain management in children, it has not been widely or effectively translated into routine clinical practice."1 Although some clinically validated methods exist (e.g. CRIES, PPIP, Faces, etc.), no "gold standard" of pain assessment has been adopted in clinical practice. All are hindered by ambiguous behavioral correlates to the pain stimuli standards as well as the subjective variability inherent in both clinical and parent evaluators 2.
Other apparatus/methods for pain assessment suffer from similar shortcomings. For example, pain tolerance threshold (PTT) and current perception threshold (CPT) determinations both rely on verbal response from a patient. Those determinations are subjective and semi-quantitative and use electrical stimulation to directly excite both large and small diameter sensory nerve fibers. The CPT determination represents the minimum amount of a potentially noxious electrical stimulus that can be perceived, while the PTT determination represents the maximum amount of noxious electrical stimulation that can be tolerated when used as a clinical diagnostic tool. Thus, PTT depends on a subject's verbal response and requires patient exposure to aversive electrical stimulation, which causes both undesirable discomfort but also elicits the affective component of pain.
Therefore, the development of tools for assessment and management of pain in newborns and children is a high priority and represents a significant unmet medical need. Both inadequately treated pain or over administration of analgesics can have deleterious physiologic consequences for neonates, infants and children. While a number of methods are in use, no "gold standard" for pain assessment exists. (Anand 2007) To accomplish meaningful pain management in children one must first be able to objectively assess pain, particularly in patients who are (1) non-verbal (e.g. neonates, infants), (2) lacking understanding and adequate verbalization skills (e.g. young children, developmentally disabled individuals) and (3) patients with compromising neuropathic clinical presentations. To address these critical issues with pain management, the Human Algometer and method are under development by Drs. Finkel and Quezado from the Pain Medicine Program at the Sheikh Zayed Institute. In brief, this device integrates a neurospecific neurostimulation of sensory nerve fibers involved in pain response and near infra-red spectroscopy (NIRS) signal acquisition derived from pain related hemodynamic changes in the somatosensory cortex. The device has the ability to collect data on the NIRS response in the cerebral cortex to noxious stimulation provided by the neurostimulation component. Signal processing of data from this trial and subsequent trials will result in (1) the detection and optimization of a NIRS signal specific to increased neuronal blood flow over the somatosensory cortex (nociceptive response) and the frontal cortex (affective component). The individual neurostimulatory and NIRS signal acquisition components integrated into this novel device are based in part or whole on previously FDA approved devices from Neurotron, Inc. and Covidien plc (former Somanetics INVOS ™) respectively.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Healthy adults | – | Device: Pressure Algometer Testing |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Healthy adults.
Key inclusion criteria (4 listed)
- the subject 18-65 years of age.
- the subject is a healthy adult with significant ongoing medical conditions
- the subject is willing to remain at the research site for the duration of the study session.
- the subject is willing and able to provide written informed consent to study participation.
Key exclusion criteria (2 listed)
- the subject has consumed alcohol within the last 12 hours prior to testing
- subject has pain at the time of testing anywhere in the body
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Pressure Algometer TestingAlso: Wagner FPIX 50™ digital pressure algometer. | Device | Healthy adults |
Primary outcome
Collection of data for signal processing that will generate the algorithms and data filters required to establish proof of concept for the novel technology.
Time frame: one year
The data collected and process from the human algometer will generate a specific NIRS nociceptive response to neurostimulation in the somatosensory cortex.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Apr 2017.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Healthy, run by Julia Finkel at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 12 Apr 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Collection of data for signal processing that will generate the algorithms and data filters required to establish proof of concept for the novel technology. (time frame: one year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Apr 2017.