Geneva, Sept. 25 -- International Clinical Trials Registry received information related to the study (NCT07830992) titled 'A Study to Evaluate Acute and Short-term Efficacy of Digest Gold on Postprandial Abdominal Distension and Subjective Bloating in Healthy Adults' on Sept. 15.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Treatment. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
Primary Sponsor: Enzymedica
Condition:
Postprandial Abdominal Distension
Bloating
Intervention:
Dietary Supplement: Digest Gold
Recruitment Status: Not recruiting
Phase: N/A
Date of First Enrollment: September 2026
Target Sample Size: ...