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Clinical Trials/NCT01088139
NCT01088139
Completed
Not Applicable

A Randomized Controlled Study of Nutritional Intervention for Geriatric Hip Fracture Patients and Its Effect on Rehabilitation Outcomes

Kowloon Hospital, Hong Kong1 site in 1 country126 target enrollmentNovember 2008
ConditionsHip Fractures

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Fractures
Sponsor
Kowloon Hospital, Hong Kong
Enrollment
126
Locations
1
Primary Endpoint
Nutritional parameters
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

This is a randomized controlled, observer blinded trial to study the beneficial effect of nutritional supplementation in elderly Hong Kong patients after hip fracture surgery during rehabilitation and at 4 weeks follow up. The control group will receive Calcium and Vitamin D supplementation whereas the intervention group will receive a moderately high dose protein nutritional supplementation in addition to Vitamin D and Calcium. Both groups undergo the same rehabilitation program and dietary counseling before discharge. They are followed up 4 weeks after discharge or completion of supplementation. The outcome parameters are nutritional parameters and rehabilitation outcomes.

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
April 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kowloon Hospital, Hong Kong

Eligibility Criteria

Inclusion Criteria

  • Age 60 years or older
  • Recent low impact osteoporotic fracture of the proximal femur surgically repaired within 4 weeks before recruitment

Exclusion Criteria

  • Patients who require tube feeding
  • Patients in unstable medical condition
  • Body mass index (BMI) ≧ 25
  • Malignancy
  • Conditions with contraindication for high protein diet
  • Mentally incapacitated and inability to communicate or understand the consent.

Outcomes

Primary Outcomes

Nutritional parameters

Time Frame: Change from Baseline in nutritional parameters at discharge from hospital and at 4 weeks after discharge

Biochemical and anthropometric measurements

Secondary Outcomes

  • Rehabilitation Outcomes(Change from Baseline in rehabilitation outcomes at discharge from hospital and at 4 weeks after discharge)

Study Sites (1)

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