High-dose Vitamin D3 in Pancreas Cancer (VITdCUT)
Primary Purpose
Pancreas Cancer, Vitamin D Deficiency, Quality of Life
Status
Terminated
Phase
Phase 3
Locations
Austria
Study Type
Interventional
Intervention
High-dose
Standard dose
Sponsored by
About this trial
This is an interventional supportive care trial for Pancreas Cancer focused on measuring V
Eligibility Criteria
Inclusion Criteria:
both sexes
- vitamin D deficiency(≤20ng/ml)
- patients>18 years of age
- pancreatic cancer
- surgical intervention/non-surgical intervention
- signed written informed consent
Exclusion Criteria:
- patients<18 years of age
- pregnancy
- contraindication for oral vitamin D intake
- hypercalcemia (> 2.65 mmol/l total calcium and/or > 1.35 mmol/l ionized calcium at screening)
- other ongoing vitamin D conducted trial
- known kidney stones, active tuberculosis or sarcoidosis (in the last 12 months)
- metastasized pancreatic cancer
- normal vitamin D serum levels
- missing written informed consent
Sites / Locations
- Medical University of Graz
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
High-dose
Standard-dose
Arm Description
Intervention with high dose oral vitamin D3 supplementation. 1 drop equals 400 I.U. This group will get 180.000 I.U. on day 1, and then 4000 I.U. per day for 60 days.
Intervention with standard dose oral vitamin D3 supplementation. 1 drop equals 400 I.U. This group will get 800 I.U. per day for 60 days.
Outcomes
Primary Outcome Measures
25(OH) vitamin D
Blood level of Vitamin D3
Secondary Outcome Measures
25(OH) vitamin D
Blood level of Vitamin D3
1,25(OH)2D vitamin D
Blood level of 1,25(OH)2D vitamin D
1,25(OH)2D vitamin D
Blood level of 1,25(OH)2D vitamin D
Urine Calcium
Calcium level in urine
Urine Calcium
Calcium level in urine
Osteocalcin
Bone marker measured in blood
Osteocalcin
Bone marker measured in blood
Beta-crosslaps
Bone marker measured in blood
Beta-crosslaps
Bone marker measured in blood
Calcium
blood measurement
Calcium
blood measurement
ionized calcium
blood measurement
ionized calcium
blood measurement
creatinine
blood measurement
creatinine
blood measurement
phosphate
blood measurement
phosphate
blood measurement
60-day mortality
Number of patients who die in the specified timeframe
hospital stay
Hospital stay in days
hospital readmission
Number of readmissions
hepcidin
blood level marker for iron status
hepcidin
blood level marker for iron status
Quality of Life questionnaire
evaluated by EORTC questionnaire
Quality of Life questionnaire
evaluated by EORTC questionnaire
Full Information
NCT ID
NCT03472833
First Posted
March 14, 2018
Last Updated
January 31, 2022
Sponsor
Medical University of Graz
1. Study Identification
Unique Protocol Identification Number
NCT03472833
Brief Title
High-dose Vitamin D3 in Pancreas Cancer
Acronym
VITdCUT
Official Title
Influence of High Dose Vitamin D3 Intake on Outcome in Pancreatic Cancer Surgery: Prospective, Randomized, Open, Controlled Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Terminated
Why Stopped
slow recruitment, patients lost to follow-up due to Covid-19 pandemic.
Study Start Date
April 1, 2018 (Actual)
Primary Completion Date
April 20, 2021 (Actual)
Study Completion Date
April 20, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Graz
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Different studies have shown that a deficiency in vitamin D (≤20ng/mL) results in higher rates in morbidity and mortality rates in cancer patients. Clinical studies investigated and demonstrated altered vitamin d tissue in pancreatic cancer. But there is no prospective study evaluating the beneficiary effects of oral supplementation of vitamin d in altered vitamin d tissue from pancreatic cancer. We want to examine the effect of a high dose vitamin D3 therapy vs. a standard base dose vitamin D3 therapy in pancreas cancer patients with a vitamin D deficiency. In case of benefit in our results we could implement vitamin D3 as a supportive standard therapy in pancreatic cancer patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreas Cancer, Vitamin D Deficiency, Quality of Life
Keywords
V
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High-dose
Arm Type
Experimental
Arm Description
Intervention with high dose oral vitamin D3 supplementation.
1 drop equals 400 I.U. This group will get 180.000 I.U. on day 1, and then 4000 I.U. per day for 60 days.
Arm Title
Standard-dose
Arm Type
Active Comparator
Arm Description
Intervention with standard dose oral vitamin D3 supplementation.
1 drop equals 400 I.U. This group will get 800 I.U. per day for 60 days.
Intervention Type
Drug
Intervention Name(s)
High-dose
Intervention Description
Patients will receive a high dose - 180.000 I.U. (1 drop equals 400 I.U.) of Vitamin D3 orally on day 1, and then 4000 I.U. for 60 days
Intervention Type
Drug
Intervention Name(s)
Standard dose
Intervention Description
Patients will receive a standard dose - 800 I.U. (equals 2 drops) of Vitamin D3 orally for 60 days
Primary Outcome Measure Information:
Title
25(OH) vitamin D
Description
Blood level of Vitamin D3
Time Frame
Day 60
Secondary Outcome Measure Information:
Title
25(OH) vitamin D
Description
Blood level of Vitamin D3
Time Frame
Day 30
Title
1,25(OH)2D vitamin D
Description
Blood level of 1,25(OH)2D vitamin D
Time Frame
Day 30
Title
1,25(OH)2D vitamin D
Description
Blood level of 1,25(OH)2D vitamin D
Time Frame
Day 60
Title
Urine Calcium
Description
Calcium level in urine
Time Frame
Day 30
Title
Urine Calcium
Description
Calcium level in urine
Time Frame
Day 60
Title
Osteocalcin
Description
Bone marker measured in blood
Time Frame
Day 30
Title
Osteocalcin
Description
Bone marker measured in blood
Time Frame
Day 60
Title
Beta-crosslaps
Description
Bone marker measured in blood
Time Frame
Day 30
Title
Beta-crosslaps
Description
Bone marker measured in blood
Time Frame
Day 60
Title
Calcium
Description
blood measurement
Time Frame
Day 60
Title
Calcium
Description
blood measurement
Time Frame
Day 30
Title
ionized calcium
Description
blood measurement
Time Frame
Day 30
Title
ionized calcium
Description
blood measurement
Time Frame
Day 60
Title
creatinine
Description
blood measurement
Time Frame
Day 30
Title
creatinine
Description
blood measurement
Time Frame
Day 60
Title
phosphate
Description
blood measurement
Time Frame
Day 60
Title
phosphate
Description
blood measurement
Time Frame
Day 30
Title
60-day mortality
Description
Number of patients who die in the specified timeframe
Time Frame
Day 60
Title
hospital stay
Description
Hospital stay in days
Time Frame
Day 60
Title
hospital readmission
Description
Number of readmissions
Time Frame
Day 60
Title
hepcidin
Description
blood level marker for iron status
Time Frame
Day 30
Title
hepcidin
Description
blood level marker for iron status
Time Frame
Day 60
Title
Quality of Life questionnaire
Description
evaluated by EORTC questionnaire
Time Frame
Day 30
Title
Quality of Life questionnaire
Description
evaluated by EORTC questionnaire
Time Frame
Day 60
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
both sexes
vitamin D deficiency(≤20ng/ml)
patients>18 years of age
pancreatic cancer
surgical intervention/non-surgical intervention
signed written informed consent
Exclusion Criteria:
patients<18 years of age
pregnancy
contraindication for oral vitamin D intake
hypercalcemia (> 2.65 mmol/l total calcium and/or > 1.35 mmol/l ionized calcium at screening)
other ongoing vitamin D conducted trial
known kidney stones, active tuberculosis or sarcoidosis (in the last 12 months)
metastasized pancreatic cancer
normal vitamin D serum levels
missing written informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Kornprat, Prof. Dr.
Organizational Affiliation
Medical University of Graz, Departement for General Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of Graz
City
Graz
State/Province
Styria
ZIP/Postal Code
8010
Country
Austria
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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High-dose Vitamin D3 in Pancreas Cancer
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