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Responsive Neurostimulation For Loss Of Control Eating
NCT03868670 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of this trial is to assess device function and safety, with secondary objectives including the feasibility.
Conditions Studied
Interventions
- DEVICE responsive neurostimulation
Study Locations (2)
California
- Stanford University — Stanford
Pennsylvania
- University of Pennsylvania — Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6 participants |
| Start Date | 2019-04-10 |
| Est. Completion | 2028-01-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03868670
The ClinicalTrials.gov registry entry for NCT03868670 describes a study currently listed as active not 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 6 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,457 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Obesity, Morbid appearing as the primary indexed condition, and to 1 intervention — of which responsive neurostimulation 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: NCT03868670 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Pennsylvania. 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 NCT03868670 about?
NCT03868670 is a clinical study titled "Responsive Neurostimulation For Loss Of Control Eating". The primary objective of this trial is to assess device function and safety, with secondary objectives including the feasibility.
What is the current status of trial NCT03868670?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 6 participants. The study started on 2019-04-10. Estimated completion is 2028-01-01.
What conditions does trial NCT03868670 study?
This clinical trial studies the following conditions: Obesity, Morbid, Loss of Control Eating. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03868670?
The interventions under investigation include: responsive neurostimulation (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03868670?
This trial is sponsored by University of Pennsylvania, which has 1,457 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03868670 being conducted?
This trial has 2 study locations across California, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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