Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING

Gastroparesis Registry 4

NCT05846802 · View on ClinicalTrials.gov ↗

Study Summary

The Gastroparesis Registry 4 (GpR4) is an observational study of patients with symptoms of gastroparesis (Gp) and functional dyspepsia (FD) with either delayed or normal gastric emptying. To better understand these disorders, this registry will capture demographic, clinical, physiological, questionnaire, and patient outcome data to characterize the patients and their clinical course. Participants will complete several questionnaires, complete a nutrient drink test and have a gastric emptying study.

Study Locations (6)

Arizona

  • Jay Pasricha — Scottsdale

Kentucky

  • University of Louisville — Louisville

Massachusetts

  • Massachusetts General Hospital — Boston

North Carolina

  • Wake Forest University and Atrium Health Carolinas Medical Center — Charlotte

Pennsylvania

  • Temple University Hospital — Philadelphia

Texas

  • Texas Tech University Health Science Center (TTUHSC) — El Paso

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2024-09-20
Est. Completion 2027-04-30

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05846802

The ClinicalTrials.gov registry entry for NCT05846802 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins Bloomberg School of Public Health, which has 209 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 6 conditions, with Gastroparesis appearing as the primary indexed condition, and to 0 interventions. 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: NCT05846802 reports 6 study locations spanning 6 distinct geographic areas — top geographies include Arizona, Kentucky, Massachusetts. 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 NCT05846802 about?

NCT05846802 is a clinical study titled "Gastroparesis Registry 4". The Gastroparesis Registry 4 (GpR4) is an observational study of patients with symptoms of gastroparesis (Gp) and functional dyspepsia (FD) with either delayed or normal gastric emptying. To better understand these disorders, this registry will capture demographic, clinical, physiological, questionn...

What is the current status of trial NCT05846802?

This trial is currently recruiting. The enrollment target is 250 participants. The study started on 2024-09-20. Estimated completion is 2027-04-30.

What conditions does trial NCT05846802 study?

This clinical trial studies the following conditions: Gastroparesis, Gastro-Intestinal Disorder, Gastroparesis Nondiabetic, Gastroparesis Due to Diabetes Mellitus Type I, Gastroparesis Due to Diabetes Mellitus Type II. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT05846802?

This trial is sponsored by Johns Hopkins Bloomberg School of Public Health, which has 209 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05846802 being conducted?

This trial has 6 study locations across Arizona, Kentucky, Massachusetts, North Carolina, Pennsylvania. 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