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RECRUITING NA

Objective Integrated Multimodal Electrophysiological Index for the Quantification of Visceral Pain

NCT06381921 · View on ClinicalTrials.gov ↗

Study Summary

The objectives of the study are to 1) Conduct telemetric biosignals (EDA, ECG, and EMG) recording in healthy controls and IBS participants experiencing cutaneous and visceral pain; and 2) Validate the OIME index as a biomarker for quantifying pain in IBS participants and its capability to assess the treatment of IBS pain via an ambulatory trial.

Conditions Studied

Interventions

  • BEHAVIORAL IBS-PPSM intervention

Study Locations (1)

Connecticut

  • Vernon Cottage, Depot Campus — Storrs

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2025-09-08
Est. Completion 2029-02-28
Phase NA

Sponsor

University of Connecticut

43 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06381921

The ClinicalTrials.gov registry entry for NCT06381921 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Connecticut, which has 43 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Abdominal Pain appearing as the primary indexed condition, and to 1 intervention — of which IBS-PPSM intervention is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06381921 reports 1 study location spanning 1 distinct geographic area — top geographies include Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06381921 about?

NCT06381921 is a clinical study titled "Objective Integrated Multimodal Electrophysiological Index for the Quantification of Visceral Pain". The objectives of the study are to 1) Conduct telemetric biosignals (EDA, ECG, and EMG) recording in healthy controls and IBS participants experiencing cutaneous and visceral pain; and 2) Validate the OIME index as a biomarker for quantifying pain in IBS participants and its capability to assess the...

What is the current status of trial NCT06381921?

This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2025-09-08. Estimated completion is 2029-02-28.

What conditions does trial NCT06381921 study?

This clinical trial studies the following conditions: Abdominal Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06381921?

The interventions under investigation include: IBS-PPSM intervention (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06381921?

This trial is sponsored by University of Connecticut, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06381921 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial