Pain Measured by NRS and EEG in Acute Pulpitis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-50
SponsorCleveland Dental Institute

About this trial

The aim of the proposed study is to investigate and comprehensively understand pain perception in patients diagnosed with symptomatic acute pulpitis who are resistant to inferior alveolar nerve block (IANB).

The study aims to achieve this by utilizing a dual approach that combines subjective self-reporting of pain intensity using the Numeric Rating Scale (NRS) with objective neurophysiological assessment through brain wave analysis using electroencephalography (EEG).

By integrating these two methods, the study seeks to explore potential correlations between self-reported pain scores and neural responses recorded through EEG, providing insights into the pain experience of this specific patient population.

Ultimately, the goal of the study is to enhance the understanding of pain perception mechanisms in individuals with symptomatic acute pulpitis resistant to IANB and potentially guide the development of more effective and personalized pain management strategies for these patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Adults male or females aged \[18-50 years\], Clinically diagnosed with symptomatic acute pulpitis based on dental examination and radiographic findings. They are medically free. They are willing and able to provide informed consent to participate in the study. They are able to communicate effectively in the language used for study procedures.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Brain wave analysis using electroencephalography (EEG).

    Diagnostic test

    Asessment of pain with objective neurophysiological assessment through brain wave analysis using electroencephalography (EEG).

  • Numerical rate Scale (NRS)

    Diagnostic test

    Asessment of pain with the subjective numercal rate scale method (NRS

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: symptomatic acute pulpitis2 interventions

Trial outcomes

Primary outcomes

1

Electroencephalography (EEG)

Changes in alpha brain waves in patients with acute pulpitis and resistant to alveolar nerve block injection

Time frame
3 months
2

Numerical Rate Scale (NRS)

Measuring pain perception using NRS (Scale 0-10 where 0 is no pain and 10 is the most unbearable pain) in patients with acute pulpitis and resistant to alveolar nerve block injection.

Time frame
3 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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