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Effects of Bisphosphonates and Nutritional Supplementation After a Hip Fracture

Primary Purpose

Hip Fracture

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Risedronate
Nutritional supplement
Calcium and vitamin D3
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hip Fracture focused on measuring Hip fracture, Nutritional supplement, Bisphosphonates, Bone mineral density, Body composition

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 60 years
  • Recent fracture of the femoral neck or trochanter
  • Without severe cognitive impairment
  • Ambulant before fracture
  • BMI ≤ 28

Exclusion Criteria:

  • Abnormal parameters regarding liver i.e. S-Alanine aminotransferase (S-ALAT) and S-Aspartate aminotransferase (S-ASAT) ≥ twice as normal
  • Abnormal parameters regarding kidney i.e. S-Creatinine > 130 µg/L
  • Primary hyperparathyroidism, osteogenesis imperfecta, Paget´s disease
  • Myeloma
  • Lactose intolerance
  • Dysphagia
  • Esophagitis
  • Gastric ulcer
  • Malignancy
  • Diabetes with nephropathy or retinopathy
  • Active iritis or uveitis

Sites / Locations

  • Department of Geriatric Medicine R94, Karolinska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Risedronate

Nutritional supplement

Calcium and vitamin D3

Arm Description

35 mg risedronate orally administered once weekly for 12 months and orally administered Calcium 1000 mg and 800 IU vitamin D3 daily for 12 months. Group B (bisphosphonate group)

Oral liquid nutritional supplement (600kcal and 40 gram protein/day) for 6 months after the hip fracture besides Risedronate and calcium and vitamin D3. Group BN (bisphosphonate and nutritional supplemented group)

An oral dose of 1000 mg Calcium and 800 IU vitamin D3 daily for 12 months after hip fracture. Group C (control)

Outcomes

Primary Outcome Measures

Total Hip Bone Mineral Density (BMD) at Baseline, 6 and 12 Months After Hip Fracture.
Total hip bone mineral density (BMD) was measured by dual-energy X-ray absorptiometry (DXA). The DXA image is two dimensional and BMD was expressed as areal density, grams per square centimeter (g/cm^2). The change in BMD between baseline, 6 and 12 months was registered.
Total Body Mineral Density (BMD) at Baseline, 6 and 12 Months After Hip Fracture.
Total body mineral density (BMD) were assessed by dual-energy X-ray absorptiometry (DXA). The DXA image is two dimensional and BMD was expressed as areal density, grams per square centimeter (g/cm^2). The change in BMD between baseline, 6 and 12 months was registered.

Secondary Outcome Measures

Body Composition, Including Lean Mass at Baseline, 6 and 12 Months After Hip Fracture.
Total body composition, including lean mass composed of muscle, visceral organs and water (LM), fat mass (FM) and bone mineral content (BMC) was measured by dual-energy X-ray absorptiometry (DXA) at baseline and at 6 and 12 months follow up. The sum of lean mass (LM) and BMC represents fat-free mass (FFM). To normalize for body size, FFM was divided by height squared to calculate fat-free mass index (FFMI, kg/m^2).
Body Composition, Including Fat Mass at Baseline, 6 and 12 Months After Hip Fracture.
Total body composition, including lean mass composed of muscle, visceral organs and water (LM), fat mass (FM) and bone mineral content (BMC) was measured by dual-energy X-ray absorptiometry (DXA) at baseline and at 6 and 12 months follow up.To normalize for body size, FM was divided by height squared to calculate fat mass index (FMI, kg/m^2).

Full Information

First Posted
September 23, 2013
Last Updated
March 20, 2021
Sponsor
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT01950169
Brief Title
Effects of Bisphosphonates and Nutritional Supplementation After a Hip Fracture
Official Title
Effects of Bisphosphonates and Nutritional Supplementation After a Hip Fracture
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study hypothesis is that nutritional supplementation together with bisphosphonates have a better preserving effect on bone mineral density (BMD) after hip fracture than bisphosphonates alone and that nutritional supplementation given postoperatively for 6 months preserve lean body mass in elderly hip fracture patients.
Detailed Description
Inclusion criteria: Men and women, ≥ 60 years of age with a recent fracture of the femoral neck or trochanter, admitted to any of the four University hospitals in Stockholm, Sweden. Patients are randomized into three groups by sealed enveloped technique in blocks by 12, thus assuring that each center had an equal distribution of patients in the three treatment groups. Patients randomly assigned and followed for 12 months. Each center with a doctor in charge and a trial nurse. The trial nurse in collaboration with the doctor are responsible of the randomization procedure and that blood samples are taken in the morning of the first weekday after inclusion at the ward and further that the dual-energy X-ray (DXA) and all estimates are done during hospital stay.The pharmacological treatment and nutritional supplementation starts as soon as the patients are circulatory stable, able to take food by mouth and are able to sit in an upright position one hour after taking the tablets.Patients are examined at baseline with a follow up at 6 and 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fracture
Keywords
Hip fracture, Nutritional supplement, Bisphosphonates, Bone mineral density, Body composition

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
79 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Risedronate
Arm Type
Active Comparator
Arm Description
35 mg risedronate orally administered once weekly for 12 months and orally administered Calcium 1000 mg and 800 IU vitamin D3 daily for 12 months. Group B (bisphosphonate group)
Arm Title
Nutritional supplement
Arm Type
Active Comparator
Arm Description
Oral liquid nutritional supplement (600kcal and 40 gram protein/day) for 6 months after the hip fracture besides Risedronate and calcium and vitamin D3. Group BN (bisphosphonate and nutritional supplemented group)
Arm Title
Calcium and vitamin D3
Arm Type
Active Comparator
Arm Description
An oral dose of 1000 mg Calcium and 800 IU vitamin D3 daily for 12 months after hip fracture. Group C (control)
Intervention Type
Drug
Intervention Name(s)
Risedronate
Other Intervention Name(s)
Bisphosphonate Group (B)
Intervention Description
The bisphosphonate group (B) receive 35 mg risedronate (Optinate® Septimum) once weekly for 12 months and calcium (1000 mg) and vitamin D3 (800 IU) (Calcichew-D3®) daily for 12 months.
Intervention Type
Other
Intervention Name(s)
Nutritional supplement
Other Intervention Name(s)
Bisphosphonate and nutritional supplemented Group (BN)
Intervention Description
The bisphosphonate and nutritional supplemented group (BN) receive 35 mg risedronate once weekly for 12 months plus nutritional supplement (Fresubin® protein energy drink) during the first six months following hip fracture and also calcium (1000 mg) and vitamin D3 (800 IU) daily for 12 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Calcium and vitamin D3
Other Intervention Name(s)
Control Group (C)
Intervention Description
The patients in the control group (C) receive orally administered calcium 1000 mg and 800 IU vitamin D3 (Calcichew-D3®) daily for 12 months.
Primary Outcome Measure Information:
Title
Total Hip Bone Mineral Density (BMD) at Baseline, 6 and 12 Months After Hip Fracture.
Description
Total hip bone mineral density (BMD) was measured by dual-energy X-ray absorptiometry (DXA). The DXA image is two dimensional and BMD was expressed as areal density, grams per square centimeter (g/cm^2). The change in BMD between baseline, 6 and 12 months was registered.
Time Frame
Baseline, 6 months and 12 months
Title
Total Body Mineral Density (BMD) at Baseline, 6 and 12 Months After Hip Fracture.
Description
Total body mineral density (BMD) were assessed by dual-energy X-ray absorptiometry (DXA). The DXA image is two dimensional and BMD was expressed as areal density, grams per square centimeter (g/cm^2). The change in BMD between baseline, 6 and 12 months was registered.
Time Frame
Baseline, 6 months and 12 months
Secondary Outcome Measure Information:
Title
Body Composition, Including Lean Mass at Baseline, 6 and 12 Months After Hip Fracture.
Description
Total body composition, including lean mass composed of muscle, visceral organs and water (LM), fat mass (FM) and bone mineral content (BMC) was measured by dual-energy X-ray absorptiometry (DXA) at baseline and at 6 and 12 months follow up. The sum of lean mass (LM) and BMC represents fat-free mass (FFM). To normalize for body size, FFM was divided by height squared to calculate fat-free mass index (FFMI, kg/m^2).
Time Frame
Baseline, 6 and 12 months
Title
Body Composition, Including Fat Mass at Baseline, 6 and 12 Months After Hip Fracture.
Description
Total body composition, including lean mass composed of muscle, visceral organs and water (LM), fat mass (FM) and bone mineral content (BMC) was measured by dual-energy X-ray absorptiometry (DXA) at baseline and at 6 and 12 months follow up.To normalize for body size, FM was divided by height squared to calculate fat mass index (FMI, kg/m^2).
Time Frame
Baseline, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 60 years Recent fracture of the femoral neck or trochanter Without severe cognitive impairment Ambulant before fracture BMI ≤ 28 Exclusion Criteria: Abnormal parameters regarding liver i.e. S-Alanine aminotransferase (S-ALAT) and S-Aspartate aminotransferase (S-ASAT) ≥ twice as normal Abnormal parameters regarding kidney i.e. S-Creatinine > 130 µg/L Primary hyperparathyroidism, osteogenesis imperfecta, Paget´s disease Myeloma Lactose intolerance Dysphagia Esophagitis Gastric ulcer Malignancy Diabetes with nephropathy or retinopathy Active iritis or uveitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margareta Hedström, MD, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Maria Sääf, MD, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Lena Flodin, MD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Geriatric Medicine R94, Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
SE-141 86
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
26572609
Citation
Flodin L, Cederholm T, Saaf M, Samnegard E, Ekstrom W, Al-Ani AN, Hedstrom M. Effects of protein-rich nutritional supplementation and bisphosphonates on body composition, handgrip strength and health-related quality of life after hip fracture: a 12-month randomized controlled study. BMC Geriatr. 2015 Nov 17;15:149. doi: 10.1186/s12877-015-0144-7.
Results Reference
derived

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Effects of Bisphosphonates and Nutritional Supplementation After a Hip Fracture

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