Gastroparesis Trial, Recruiting NCT07720323 Sponsor: Ohio State University Condition: Gastroparesis
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Gastroparesis Trial, Recruiting

NCT07720323
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been experiencing nausea for more than 2 months
  • People who are 18 years of age or older
  • People who are able to understand English
  • People who are currently receiving care at The Ohio State University
  • People who are able to complete online surveys using a smartphone or computer

Who may not be able to join:

  • People who are currently undergoing treatment for cancer
  • People who are currently being treated for inflammatory bowel disease
  • People who have cirrhosis (serious liver scarring)
  • People who have end-stage renal (kidney) disease
  • People who have previously used a wearable TENS device (a small electrical stimulation device worn on the body) for nausea
  • People who have had abdominal surgery within the last 3 months
  • People who are pregnant (as reported by the individual at the time of enrollment)
  • People who currently have carpal tunnel syndrome (a nerve condition affecting the wrist and hand)
  • People for whom the EmeTerm wrist device would not be medically appropriate to use (confirm with trial site)
  • People who have skin problems near the wrist where the device would be worn, such as inflammation, irritation, infection, sores, bleeding, or open wounds
  • People who have any metallic implants in their body
  • People who have had a head or facial injury within the last 3 months
  • People who have a known brain tumor, meningitis, or have had a stroke within the last 3 months
  • People who have a cardiac pacemaker, an implanted defibrillator, or any other implanted metallic or electronic device
  • People who have a history of seizures

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Subhankar CHAKRABORTY, MD, Ph.D., Ohio State University

Phone: 614-293-6255'

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Ohio State University
Registry
ClinicalTrials.gov
Start date
1 February 2023
Est. completion
31 December 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in Average Weekly Frequency of Moderate to Severe Nausea

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov