The Effect of Supplementation of Vitamin D Deficiency in Older People With Acute Hip Fracture:

PHASE4CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

January 1, 2018

Primary Completion Date

April 20, 2019

Study Completion Date

July 30, 2020

Conditions
Hip FractureVitamin D Deficiency
Interventions
DRUG

Calcifediol (Vitamin D)

"After surgical treatment, participants with vitamin D deficiency (25OHD \< 30 ng/mL) will be randomly allocated to an intervention group or control group.~For the intervention group, participants will receive 16. 000 U oral Calcifediol daily for 5 days.~For the control group, participants will receive 16.000 U oral Calcifediol weekly for 5 weeks.~Both groups:~1. Will follow the usual hip fracture rehabilitation pathway.~2. 25OHD serum levels will be measured after 4 weeks. Depending on the serum 25OHD level, the patients will receive different vitamin D strategies (according to the protocol) Patients will be monitored for up to 12 months after the discharge from the hospital, with 3 clinic visits at 3, 6 and 12 months (to determine serum vitamin D levels and to evaluate functional status)"

Trial Locations (1)

08227

Consorci Sanitari de Terrassa, Terrassa

All Listed Sponsors
collaborator

Fundacio Salut i Envelliment UAB

OTHER

lead

Leonor Cuadra Llopart

OTHER

NCT03213886 - The Effect of Supplementation of Vitamin D Deficiency in Older People With Acute Hip Fracture: | Biotech Hunter | Biotech Hunter