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NCT05846802 · ClinicalTrials.gov registry record
Gastroparesis Registry 4
A clinical trial of Gastroparesis and Gastro-Intestinal Disorder, sponsored by Johns Hopkins Bloomberg School of Public Health.
- Recruiting
- Registry status
- 250
- Enrollment target
- 6
- Study locations
NCT05846802: Recruiting study of Gastroparesis and Gastro-Intestinal Disorder, sponsored by Johns Hopkins Bloomberg School of Public Health.
NCT05846802 is a study of Gastroparesis and Gastro-Intestinal Disorder that is actively recruiting participants, run by Johns Hopkins Bloomberg School of Public Health. The registered enrollment target is 250 participants, below the 296-participant average among 44 other Gastroparesis trials with a reported enrollment target (16% lower). The trial reports 6 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05846802, a study of Gastroparesis and Gastro-Intestinal Disorder, is actively recruiting participants, sponsored by Johns Hopkins Bloomberg School of Public Health.
- RECRUITING
- Registry status
- 250 participants
- Enrollment target
- 6
- Study locations
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.
Primary Outcome
Change in PAGI-SYM total score from baseline to 48 weeks. The final PAGI-SYM contains 20 items grouped into 6 subscales covering: heartburn/regurgitation (7 items), nausea/vomiting (3 items), post-prandial fullness/early satiety (4 items), bloating (2 items), upper abdominal pain (2 items), and lower abdominal pain (2 items). A 6-point Likert response scale, ranging from 0 (none) to 5 (very severe), is used for rating the severity of each symptom item over a 2-week recall period. * Subscale sc
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 250 participants |
| Start Date | 2024-09-20 |
| Est. Completion | 2027-04-30 |
What NCT05846802 shows while recruiting
NCT05846802 is an observational study that tracks outcomes without assigning an intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 296-participant average among 44 other Gastroparesis trials with a reported enrollment target (16% lower).
The record links to 6 conditions, with Gastroparesis appearing as the primary indexed condition, and to 0 interventions.
NCT05846802 lists 6 locations in 6 states (Arizona, Kentucky, Massachusetts).
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.
Who is sponsoring clinical trial NCT05846802?
This trial is sponsored by Johns Hopkins Bloomberg School of Public Health, which has 187 total clinical trials registered on ClinicalTrials.gov.
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.
Learn More About Clinical Trials
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Where NCT05846802's enrollment target sits among peer trials
250 9th of 44 higher than 35 of 44 other Gastroparesis trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Gastroparesis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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