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Completed

NCT Number: NCT07445633

The Ability of Brain Waves Activity to Detect Patient Susceptibility to Post-Operative Pain

This observational study evaluates whether resting-state EEG alpha activity can help identify endodontic patients at higher risk of post-operative pain following single-visit root canal treatment. EEG will be recorded before treatment and pain intensity will be self-reported using a Visual Analogue Scale (VAS) during the early post-treatment period.

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Key information

Age range

20 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Ain Shams University

Cairo, Egypt

About this study

This observational clinical study is designed to examine the association between resting-state electroencephalography (EEG) alpha activity and the intensity of post-operative pain following single-visit root canal treatment. Participants will be recruited from an endodontic clinic after ethics committee approval. Resting-state EEG will be recorded using a wearable EEG system prior to treatment. Post-operative pain intensity will be assessed using a patient-reported Visual Analogue Scale (VAS) during the early post-treatment period.

Participants will be classified based on baseline alpha activity (e.g., lower versus higher alpha power range). Analyses will evaluate whether baseline EEG alpha measures are associated with subsequent pain ratings and whether differences in alpha activity relate to higher post-operative pain susceptibility. The goal is to determine whether EEG alpha activity may serve as a practical biomarker for post-endodontic pain susceptibility.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient's age ranges from 20-40.
  • Vital lower first molar with signs and symptoms of acute irreversible pulpitis and indicated for single visit root canal treatment.
  • Patients that had not received any medicinal therapy after endodontic treatment.
  • Patients who are mentally and physically capable to record pain intensity estimated every 6 hours after endodontic treatment using VAS.

Exclusion criteria

  • Patient systemic disease or neurogenic disease that contraindicates the use of the EEG or have sensitivity to the electrode material.
  • Cases that root canal treatment could not be finished in a single visit such as teeth with apical periodontitis, pulpal necrosis, chronic apical abscess.
  • Patients who took analgesics within 24 hours after endodontic treatment.

Treatment and study plan

Detection of th alpha brain waves activity

Diagnostic Test

The study utilizes the EMOTIV® EPOC X, a mobile, wireless 14-channel EEG headset. This differs from traditional clinical EEG setups that often require bulky, wired equipment and the application of messy conductive gels, making this method much more suitable for a chair-side dental environment.

Primary outcomes

  1. brain wave activity

    Time frame: 24 hours

    The primary outcome is the correlation between pre-operative brain wave activity and post-operative pain intensity

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Mar 3, 2026
Registry last updated
Mar 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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