Probiotics Regulates Skin Care in Children

NCT ID: NCT05005611

Last Updated: 2023-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

148 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-31

Study Completion Date

2024-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Probiotics, a component that is generally referred to as a living microorganism or a microorganism present in a host. Most studies have shown that probiotics can regulate immune function in the body. Many studies have attempted to understand whether the use of probiotics can prevent allergic diseases or not.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Skin Care Probiotics Children

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Skin Care in children.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Investigators
Double-blind.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

A pack of powder without probiotics.

1 pack / day

Probiotics Lactobacillus salivarius AP-32

Group Type EXPERIMENTAL

Probiotics Lactobacillus salivarius AP-32

Intervention Type DIETARY_SUPPLEMENT

A pack of powder with probiotics Lactobacillus salivarius AP-32

1 pack / day

Probiotics Bifidobacterium animalis subsp. lactis CP-9

Group Type EXPERIMENTAL

Probiotics Bifidobacterium animalis subsp. lactis CP-9

Intervention Type DIETARY_SUPPLEMENT

A pack of powder with probiotics Bifidobacterium animalis subsp. lactis CP-9

1 pack / day

Probiotics Lactobacillus rhamnosus LGG

Group Type EXPERIMENTAL

Probiotics Lactobacillus rhamnosus LGG

Intervention Type DIETARY_SUPPLEMENT

A pack of powder with probiotics Lactobacillus rhamnosus LGG

1 pack / day

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Placebo

A pack of powder without probiotics.

1 pack / day

Intervention Type DIETARY_SUPPLEMENT

Probiotics Lactobacillus salivarius AP-32

A pack of powder with probiotics Lactobacillus salivarius AP-32

1 pack / day

Intervention Type DIETARY_SUPPLEMENT

Probiotics Bifidobacterium animalis subsp. lactis CP-9

A pack of powder with probiotics Bifidobacterium animalis subsp. lactis CP-9

1 pack / day

Intervention Type DIETARY_SUPPLEMENT

Probiotics Lactobacillus rhamnosus LGG

A pack of powder with probiotics Lactobacillus rhamnosus LGG

1 pack / day

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Estimated by PI.

Exclusion Criteria

* Be allergic to medicine
* Take medicine like immune inhibition, or steroid injection in two weeks
* Participate in another clinical research or immune therapy in one month
* Have severe disease
* Inappropriate for this trial judged by PI
Minimum Eligible Age

1 Year

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Glac Biotech Co., Ltd

INDUSTRY

Sponsor Role collaborator

Chang Gung Memorial Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ho-Chang Kuo

Attending Physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Kaohsiung Chang Gung Memorial Hospital

Kaohsiung City, , Taiwan

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Taiwan

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Kuo Ho-Chang

Role: CONTACT

(07)7317123 ext. 8320

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Ho-Chang Kuo, MD, PhD

Role: primary

+886-7-7317123 ext. 8320

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

XPRPG8L0021~22

Identifier Type: -

Identifier Source: org_study_id

NCT05337670

Identifier Type: -

Identifier Source: nct_alias

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Probiotics and Allergic Diseases
NCT01635738 COMPLETED NA