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Therapeutic Benefit of Preoperative Supplemental Vitamin D in Patients Undergoing Major Surgical Procedures.

Primary Purpose

Vitamin d Deficiency

Status
Withdrawn
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Blood draw pre-operatively
Blood draw post-operative Day 1
Blood draw post-operative Day 2
Sponsored by
University of Missouri, Kansas City
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vitamin d Deficiency focused on measuring vitamin d deficiency, cathelicidin antimicrobial peptide, resistin, human, protein, human, 1,25-dihydroxy-16,23-diene vitamin D3, Cholecalciferol, Nutritional Status, length of stay

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • English Speaking
  • Age 18 years or older
  • Patient undergoing major elective surgery with planned open abdominal incisions, and planned hospitalization of two days or longer.

Exclusion Criteria:

  • Pregnant
  • Non-English Speaking
  • Chronic severe kidney disease (Stage III, IV, V)

Sites / Locations

  • Truman Medical Center Hospital Hill

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vitamin D3

Placebo pill

Arm Description

Vitamin D3 (cholecalciferol) 50,000 IU by mouth daily for each of the five days prior to surgery. Blood draw pre-operatively Blood draw post-operative Day 1 Blood draw post-operative Day 2

Placebo pill by mouth daily for each of the five days prior to surgery. Blood draw pre-operatively Blood draw post-operative Day 1 Blood draw post-operative Day 2

Outcomes

Primary Outcome Measures

Change in Vitamin D level as measured as 25-OHD level
Change in Vitamin D level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2

Secondary Outcome Measures

Change in Resistin level in the blood
Change in Resistin level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2
Change in Cathelicidin level in the blood
Change in Cathelicidin level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2
Change in Calcium Level in the blood
Change in Calcium level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2

Full Information

First Posted
April 9, 2014
Last Updated
June 14, 2017
Sponsor
University of Missouri, Kansas City
Collaborators
Truman Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02138591
Brief Title
Therapeutic Benefit of Preoperative Supplemental Vitamin D in Patients Undergoing Major Surgical Procedures.
Official Title
Therapeutic Benefit of Preoperative Supplemental Vitamin D in Patients Undergoing Major Surgical Procedures.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Withdrawn
Study Start Date
February 2016 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri, Kansas City
Collaborators
Truman Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Vitamin D (Vitamin D) deficiency is very common. We recently showed that 97% of 204 patients admitted to Truman Medical Center were Vitamin D deficient (<30 ng/ml). However, the consequences of Vitamin D deficiency, particularly with respect to infection, are not well understood. It is known that production of cathelicidin, an important antimicrobial peptide, is critically dependent upon Vitamin D. It is also established that levels of cathelicidin correlate inversely with urinary tract infection risk. We hypothesize that restoration of Vitamin D levels to normal in patients undergoing major surgery will result in significant decreases in levels of perioperative infections due to restoration of normal levels of circulating Vitamin D, which in turn will elevate cathelicidin levels. As an initial test of this hypothesis, we propose a double-blind, prospective, randomized study of pre-operative Vitamin D supplementation. Fifty subjects undergoing surgery will receive daily Vitamin D3 (50,000 IU) for five days pre-operatively, with controls receiving placebo. Levels of Vitamin D, calcium, cathelicidin, and the pro-inflammatory protein resistin, will be monitored before Vitamin D supplementation (pre-operatively) and after Vitamin D supplementation (post-operative days 1 and 2). The effect of these changes should be to decrease the incidence of infectious complications. We expect to observe Vitamin D levels increase to normal, and cathelicidin levels become elevated. We expect to see increased levels of resistin in patients developing infections. This study will provide strong pilot evidence for future NIH funding.
Detailed Description
The long term goal in our research is to develop and implement effective, evidence-and mechanism-based interventions to improve outcomes for surgical and trauma patients. Of potential importance, findings from our own recent pilot studies have established that > 95% of patients seen at Truman Medical Center (TMC) are seriously Vitamin D deficient with plasma levels significantly lower than normal. Our objective in this application, therefore, is to assess the short term therapeutic benefit of high dose Vitamin D in patients admitted to TMC for elective major abdominal surgery. We propose to measure plasma Vitamin D and Calcium levels before supplementation (pre-operatively), and after supplementation (post-operatively), and monitor the biomarker proteins cathelicidin and resistin at the same times. Data on Vitamin D levels will be used to assess direct biochemical effects. Measurement of cathelicidin levels will provide additional information. Since Vitamin D has been shown to induce increased expression of this antimicrobial protein. Monitoring of circulating levels of resistin provides a highly sensitive early measure of infection (unpublished observations). Calcium levels will also be monitored since there is a significant chance that pre-operative calcium levels will be low in some patients, and that supplementation with vitamin D may increase the calcium level. Measures of secondary clinical outcomes will include length of hospital stay and incidence of post-operation infection. Our central hypothesis is that, relative to patients receiving peri-operative standard of care, patients receiving 250,000 units of Vitamin D pre-operatively will manifest levels of Vitamin D to within the normal range and will have elevated levels of cathelicidin. We further hypothesize that patients receiving Vitamin D will have reduced incidence of infection, which will correlate with lower levels of resistin, and will exhibit trends toward shorter hospital stay. Our proposed specific aims are: Specific Aim #1: Determine biochemical consequences of Vitamin D supplementation in elective surgery patients We hypothesize that preoperative supplementation with high dose Vitamin D will result in levels of Vitamin D in treated patients within the normal range, corresponding with significant increases in plasma levels of cathelicidin, relative to control patients receiving standard of care. Specific Aim # 2: Evaluate clinical benefits of Vitamin D supplementation in post-elective surgery patients We postulate that patients given Vitamin D will trend toward lower rates of post-surgery infection, as evidenced by the absence of circulating resistin and decreased detection of pulmonary or wound-site infection, and will have shorter hospital stays relative to patients receiving standard of care. It is our expectation that, at the completion of this pilot study, we will have provided strong evidence that plasma levels of Vitamin D, as measured by 25-OHD, can be reproducibly raised to normal levels as measured in post-surgery patients and that the administered Vitamin D will have detectable biochemical benefits. We further expect that, while the power of the proposed study will not be sufficient for statistically valid results, there will be trends toward clinical benefits in Vitamin D treated patients. Collectively, these findings would provide strong evidence to support feasibility of an NIH-supported Phase I trial to assess Vitamin D benefits in surgery and/or trauma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin d Deficiency
Keywords
vitamin d deficiency, cathelicidin antimicrobial peptide, resistin, human, protein, human, 1,25-dihydroxy-16,23-diene vitamin D3, Cholecalciferol, Nutritional Status, length of stay

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D3
Arm Type
Experimental
Arm Description
Vitamin D3 (cholecalciferol) 50,000 IU by mouth daily for each of the five days prior to surgery. Blood draw pre-operatively Blood draw post-operative Day 1 Blood draw post-operative Day 2
Arm Title
Placebo pill
Arm Type
Placebo Comparator
Arm Description
Placebo pill by mouth daily for each of the five days prior to surgery. Blood draw pre-operatively Blood draw post-operative Day 1 Blood draw post-operative Day 2
Intervention Type
Procedure
Intervention Name(s)
Blood draw pre-operatively
Other Intervention Name(s)
Venipuncture
Intervention Description
Pre-Operative blood draw of approximately 32ml will check the following: Vitamin D (25-OHD), Calcium, Cathelicidin and Resistin levels in the blood.
Intervention Type
Procedure
Intervention Name(s)
Blood draw post-operative Day 1
Other Intervention Name(s)
Venipuncture
Intervention Description
Blood draw of approximately 32ml to check the following: Vitamin D (25-OHD), Calcium, Cathelicidin and Resistin levels in the blood.
Intervention Type
Procedure
Intervention Name(s)
Blood draw post-operative Day 2
Other Intervention Name(s)
Venipuncture
Intervention Description
Blood draw of approximately 32ml to check the following: Vitamin D (25-OHD), Calcium, Cathelicidin and Resistin levels in the blood.
Primary Outcome Measure Information:
Title
Change in Vitamin D level as measured as 25-OHD level
Description
Change in Vitamin D level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2
Time Frame
Pre-operatively, Post-operative Day 1 and Postoperative Day 2
Secondary Outcome Measure Information:
Title
Change in Resistin level in the blood
Description
Change in Resistin level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2
Time Frame
Pre-operatively, Post-operative Day 1, Post-operative Day 2
Title
Change in Cathelicidin level in the blood
Description
Change in Cathelicidin level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2
Time Frame
Pre-operatively, Post-operative Day 1, Post-operative Day 2
Title
Change in Calcium Level in the blood
Description
Change in Calcium level from Pre-Operatively to Post-Operative Day 1 and Post-Operative Day 2
Time Frame
Pre-operatively, Post-operative Day 1, Post-operative Day 2

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English Speaking Age 18 years or older Patient undergoing major elective surgery with planned open abdominal incisions, and planned hospitalization of two days or longer. Exclusion Criteria: Pregnant Non-English Speaking Chronic severe kidney disease (Stage III, IV, V)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles Van Way III, M.D.
Organizational Affiliation
Truman Medical Center and University of Missouri Kansas City
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Dustin Neel, MD
Organizational Affiliation
Truman Medical Center and University of Missouri Kansas City
Official's Role
Principal Investigator
Facility Information:
Facility Name
Truman Medical Center Hospital Hill
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22206852
Citation
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Citation
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Results Reference
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PubMed Identifier
21443793
Citation
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Results Reference
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Citation
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Results Reference
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22975885
Citation
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Citation
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Citation
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Citation
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Therapeutic Benefit of Preoperative Supplemental Vitamin D in Patients Undergoing Major Surgical Procedures.

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