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LL-37

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

Quick Stats
Studies 2230
Trials 95
Completed PHASE2 INTERVENTIONAL NCT01689441

Randomized Controlled Trial of Calcitriol vs. Placebo Among Critically-ill Patients With Sepsis

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Observational studies among critically ill patients have shown strong associations between vitamin D deficiency and adverse outcomes, including increased length of stay, infection, and mortality. It is unknown whether vitamin D deficiency contributes directly to adverse outcomes or whether it is simply a biomarker of severity of illness or overall health status. However, vitamin D plays a key role in host defense, largely by stimulating production of the anti-microbial peptide cathelicidin (LL-37). We will test the hypothesis that administration of activated vitamin D (calcitriol) will increase serum levels of cathelicidin.

Interventions

Name: Calcitriol
Type: DRUG
Description:
Name: Placebo
Type: DRUG
Description:

Primary Outcomes

Measure: Plasma Cathelicidin (hCAP18) Protein Levels at 48 Hours
TimeFrame: 48 hours
Description:

Trial Information

NCT ID

NCT01689441

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

Brigham and Women's Hospital

Last Updated

December 15, 2025