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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Not Yet Recruiting NA INTERVENTIONAL NCT06863415

Study on the Enhancement of Intestinal and Immune Functions Through Probiotic Intervention

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Evaluate the effectiveness and safety of Bifidobacterium longum subsp. infantis BI45 as a food supplement compared to a placebo in improving intestinal and immune functions in healthy adults.

Interventions

Name: Probiotic
Type: DIETARY_SUPPLEMENT
Description: Dietary supplement: Probiotics. The trial period of this study lasts for 2 months (8 weeks), during which each participant will have 3 visits (at month 0, month 1, and month 2).
Name: Placebo
Type: DIETARY_SUPPLEMENT
Description: Dietary supplement: Placebo. The trial period of this study lasts for 2 months (8 weeks), during which each participant will have 3 visits (at month 0, month 1, and month 2).

Primary Outcomes

Measure: Change in the concentration of antimicrobial peptides (LL-37 and calprotectin) in feces before and after intervention
TimeFrame: Week 0 and Week 8
Description: Detected by Enzyme-Linked Immunosorbent Assay (ELISA).

Trial Information

NCT ID

NCT06863415

Status

Not Yet Recruiting

Study Type

INTERVENTIONAL

Phases

NA

Sponsor

Wecare Probiotics Co., Ltd.

Last Updated

December 15, 2025