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HealthyNCT02325284

Objective Measurement of Pain Using the Algometer

An observational study of Healthy, run by Julia Finkel at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in United States

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 groups in NCT02325284
Study groupRoleWhat they receive
Healthy adultsNot described
Receives: Device: Pressure Algometer Testing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

  1. First posted24 Dec 2014 (estimated)
  2. Study startSep 2014
  3. Primary completionSep 2016
  4. Study completionDec 2016

Resources

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)
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

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.

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