LivingGLP1
Study S001783

A Study to Evaluate the Effect of Fasting Duration and Temporary Withholding of Dulaglutide on Retained Gastric Contents Using Gastric Ultrasound in Participants With Type 2 Diabetes Mellitus

Registration

Registration
NCT07313813
Acronym
GBGT
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
20
Start
2025-12-29
Primary completion
2026-08-13
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes Mellitus (T2DM)
Interventions
DRUG:Dulaglutide
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:H9X-MC-GBGT

Registered primary outcomes

  • Percentage of Fasting Participants with Lack of Gastric Content Retention Post-Solid Test Meal [Day 116 (at 6, 8, 12, 18 and 24 hours after baseline or Day 115 solid test meal)]

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