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GCWB1001 Evaluates the Effectiveness and Safety of Respiratory Health

NCT05544942 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2026-02-23

No results posted yet for this study

Summary

This human application test was designed to evaluate the effectiveness and safety of the losing suction tendon, compared to the control food when the GCWB1001 was consistent with the symptoms of the respiratory symptoms of mildness.

Conditions

  • Respiratory Symptoms

Interventions

DIETARY_SUPPLEMENT

Lactobacillus plantarum

1 capsule once a day

OTHER

maltodextrin

1 capsule once a day

Sponsors & Collaborators

  • Green Cross Wellbeing

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
69 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-23
Primary Completion
2023-08-30
Completion
2023-08-31

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05544942 on ClinicalTrials.gov