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Study identifier: NCT05199441 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

Efficacy of Galeo® in Patients With Postprandial Distress Syndrome Subtype in Functional Dyspepsia

Condition: Dyspepsia  ·  Sponsor: Pusan National University Yangsan Hospital

PhasePhase 4
Planned participants226
Who can joinAll sexes, 19 Years to no upper limit
Healthy volunteersNo

About this study

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Galeo® on dyspepsia symptoms in patients with postprandial distress syndrome subtype in functional dyspepsia for 8 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (6)

Pusan National University Yangsan HospitalYangsan, Gyeungsangnam-do, South Korea
Hallym University Sacred Heart HospitalAnyang, South Korea
Dong-A University HospitalBusan, South Korea
Chungnam National University HospitalDaejeon, South Korea
Korea University Guro HospitalSeoul, South Korea
Koreal University Anam HospitalSeoul, South Korea

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