MedPath

Regime for Vitamin D Maintenance in Post-Operative Patients

Phase 3
Not yet recruiting
Conditions
Sarcopenia
Interventions
Registration Number
NCT06708741
Lead Sponsor
Sengkang General Hospital
Brief Summary

Vitamin D plays a significant part calcium and phosphate haemostasis, thus, intrinsically critical for bone health. Increasing evidence also reveal that insufficient serum vitamin D levels also result in poor muscle health with such individuals having a compromised muscle building potential (4 times slower muscle building).

Muscle health is a critical component of a post-surgical patient recovery, with impaired muscle function leading to reduced functional ability, resulting in a poorer quality of life. Poor muscle health also has negative repercussion on survivability, with reduced overall, and disease-specific survival, especially shown in cancer patients. Thus, maintenance of vitamin D levels post-surgery may be more critical than previously thought.

Detailed Description

This study is performed in Singapore (outside the US) and the medication, while it is a FDA approved medication, is not manufactured in the US for the trial purpose and the indications of use in this trial is not new.

The investigators would be recruiting patients aged 21-65 years who have undergone major surgery (defined by the NICE criteria) and who are able to provide informed consent, accept to take vitamin D supplements post-operatively and have their serum vitamin D levels checked periodically.

The investigators will excluded patients who have undergone minor procedures (Table code \<4a), those who have a history of chronic kidney disease/end staged renal failure, known hyperparathyroidism, are non-ambulatory independently and have had known allergies to the commercially available high dose vitamin D formulations.

High dose oral vitamin D supplementation (50,000 IU/week for 8 weeks) is the current recommended dose for individuals with vitamin D insufficiency of deficiency and is currently being used for some prehabilitation programmes due to the quick repletion of vitamin D levels to improve muscle gain during the short prehabilitation window prior to surgery.

Using the same dose once a month would provide a significantly less vitamin D supplementation, especially with individuals who have had their vitamin D levels repleted in the preoperative phase. This will be compared against a control who are randomised to standard-of-care (SOC) where high dose vitamin D maintenance is not prescribed.

The unmet clinical need is the still unknown, unstandardised vitamin D supplementation regime. There are current no clinical consensus on vitamin D supplementation after patients who have undergone major surgery.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Serum 25-hydroxyvitamin D levels between 30-50ng/ml at 4-6 weeks after operation
  • aged 21-65 years
  • ability to provide informed consent
  • accepts to take vitamin D supplements post-operatively and
  • have their serum vitamin D levels checked periodically.
Exclusion Criteria
  • They have undergone minor procedures (Table code <4a)
  • have a history of chronic kidney disease/end staged renal failure
  • have previous history of ureteric/kidney stones
  • known hyperparathyroidism
  • are non-ambulatory independently
  • have had known allergies to the commercially available high dose vitamin D formulations.
  • Vulnerable personnel would be excluded from the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vitamin D supplementationVitamin DHigh dose oral vitamin D supplementation (50,000 IU/once a month)
Primary Outcome Measures
NameTimeMethod
serum 25-hydroxyvitamin D levels at 3-months post-intervention3 months after initiation

serum 25-hydroxyvitamin D levels at 3-months post-intervention

Secondary Outcome Measures
NameTimeMethod
functional outcome measures at 6-months post-intervention6 months after initiation

functional outcome measures at 6-months post-intervention

functional outcome measures at 12-months post-intervention12 months after initiation

functional outcome measures at 12-months post-intervention

functional outcome measures at 3-months post-intervention3-months after intiation

functional outcome measures at 3-months post-intervention

serum 25-hydroxyvitamin D levels compared to SOC at 6-months post-intervention.6 months after initiation

serum 25-hydroxyvitamin D levels compared to SOC at 6-months post-intervention.

serum 25-hydroxyvitamin D levels compared to SOC at 12-months post-intervention.12 months after initiation

serum 25-hydroxyvitamin D levels compared to SOC at 12-months post-intervention.

muscle quality (Ultrasound+MuscleSound™ evaluation) at 3-months post-intervention3 months after intiation

muscle quality (Ultrasound+MuscleSound™ evaluation) at 3-months post-intervention

muscle quality (Ultrasound+MuscleSound™ evaluation) at 6-months post-intervention6 months after initiation

muscle quality (Ultrasound+MuscleSound™ evaluation) at 6-months post-intervention

muscle quality (Ultrasound+MuscleSound™ evaluation) at 12-months post-intervention12 months after initiation

muscle quality (Ultrasound+MuscleSound™ evaluation) at 12-months post-intervention

quality of life (EQ5D-3L) at 3-months post-intervention3 months after intiation

quality of life (EQ5D-3L) at 3-months post-intervention

quality of life (EQ5D-3L) at 6-months post-intervention6 months after initiation

quality of life (EQ5D-3L) at 6-months post-intervention

quality of life (EQ5D-3L) at 12-months post-intervention12 months after initiation

quality of life (EQ5D-3L) at 12-months post-intervention

Trial Locations

Locations (1)

Sengkang General Hospital

🇸🇬

Singapore, Singapore

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