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ll-37 antimicrobial peptide rct 2013-01 ClinicalTrials

High-Dose Vitamin D Supplementation Explored for Colorectal Surgery Patients

High Dose Preoperative Cholecalciferol Supplementation and Perioperative Vitamin D Status

Background

Robust postoperative immune function is critical for patient recovery and reducing the risk of surgical site infections (SSIs). Concurrently, vitamin D is increasingly recognized as a key regulator of both the innate and adaptive immune systems. This study addresses the knowledge gap of whether high-dose preoperative cholecalciferol supplementation can effectively improve perioperative vitamin D status in colorectal surgery patients, a population historically at higher risk for developing SSIs.

Results

The provided research record describes the design and rationale of this completed study (NCT01689779) but does not report the actual results or specific data points regarding vitamin D status changes or patient outcomes. Therefore, no specific findings, percentages, or p-values can be presented from this abstract. The primary objective of this study was to determine if high-dose preoperative cholecalciferol supplementation, specifically a 100,000 IU dose, could significantly improve perioperative vitamin D status in colorectal surgery patients compared to a placebo group. The study was designed to measure the effect of the intervention on circulating 25-hydroxyvitamin D levels, which is the main indicator of vitamin D status. Without the reported results, we cannot quantitatively compare the treatment versus control groups' actual outcomes.

Why It Matters

This study's design highlights the potential for nutritional intervention to support surgical recovery by optimizing a key immune modulator. If positive results were found, optimizing vitamin D levels could become a standard preoperative strategy to enhance immune function and potentially reduce complications like SSIs. Future research would then need to confirm these benefits in larger cohorts and assess direct impacts on infection rates, potentially leading to Phase II or III human trials to establish clinical efficacy.


ll-37 antimicrobial peptide cathelicidin immune-function dose mentioned
Source: clinicaltrials:NCT01689779 · Ingested 2026-04-07 · Digest: gemini-2.5-flash