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Effect of Vitamin D in Burn Patients

H

Hangang Sacred Heart Hospital

Status

Unknown

Conditions

Burn Surgery

Treatments

Biological: Vitamin D

Study type

Interventional

Funder types

Other

Identifiers

NCT03884036
2019-003

Details and patient eligibility

About

The purpose of this study is to evaluate pre-operative vitamin D levels in patients with burn injuries and evaluate the effect of vitamin D on postoperative complications and duration of hospitalization.

Full description

Vitamin D deficiency often occurs in burn patients, which may include longer hospitalization and respiratory and cardiac complications.

The purpose of this study is to evaluate pre-operative vitamin D levels in patients with burn injuries and evaluate the effect of vitamin D on postoperative complications and duration of hospitalization.

Enrollment

264 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • vitamin D <30 ng/ml
  • patients undergoing burn surgery

Exclusion criteria

  • age < 18 years old
  • hypercalcemia
  • renal disease
  • cardiac disease ( EF<40%, MI, angina)
  • respiratory disease (ARDS, pneumonia)
  • intubated patients
  • electrical burn

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

264 participants in 2 patient groups, including a placebo group

Vitamin D group
Active Comparator group
Description:
Vitamin D 200,000 IU (1 cc) IM
Treatment:
Biological: Vitamin D
Control group
Placebo Comparator group
Description:
Normal saline 1 cc IM
Treatment:
Biological: Vitamin D

Trial contacts and locations

1

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Central trial contact

Hee Yeong Kim, MD

Data sourced from clinicaltrials.gov

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