NCT07172607

The Effect of Avnace eZZe on Sleep Improvement

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 75 (estimated)
• Sponsor: TCI Co., Ltd. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

This study aims to examine the effectiveness of Avance eZZe drink with liposomal technology in improving sleep quality. Participants will be randomly assigned to either the placebo group, Avance eZZe drink group, and Avance eZZe drink without liposomal group, with 25 participants in each group. On the day of the experiment (day 0), participants are required to fill out questionnaires assessing sleep disorders and stress condition, and use a sleep monitoring system to track their sleep and autonomic nervous system conditions. Subsequently, participants will be given the experimental samples and instructed to consume them 1 hour before sleep daily for 28 days. Follow-up assessments will be conducted in the day-1, day-14 and day-28, participants are required to fill out questionnaires assessing sleep disorders and stress condition, and use a sleep monitoring system to track their sleep and autonomic nervous system conditions.

Conditions

• Sleep Disorder (Disorder)
• Anxiety Depression Disorder

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	Avance eZZe drink	25 mL liquid sachet, 1 sachet/day, consume 1 sachet of the sample 1 hour before sleep daily
DIETARY_SUPPLEMENT	Avance eZZe drink (without liposomal)	25 mL liquid sachet, 1 sachet/day, consume 1 sachet of the sample 1 hour before sleep daily
DIETARY_SUPPLEMENT	Placebo drink	25 mL liquid sachet, 1 sachet/day, consume 1 sachet of the sample 1 hour before sleep daily

Timeline

• Start date: 2025-09-09
• Primary completion: 2026-04-30
• Completion: 2026-06-30
• First posted: 2025-09-15
• Last updated: 2026-02-04

Locations

1 site across 1 country: Taiwan