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The Effectiveness of Two Osteoporosis Drugs on Prosthetic Bone Mineral Density (BMD) Loss After Total Hip Arthroplasty(THA) (ETOD)

Y

Yokohama City University Medical Center

Status

Unknown

Conditions

Arthroplasty, Replacement, Hip
Bone Density

Treatments

Drug: alendronate, alfacalcidol

Study type

Interventional

Funder types

Other

Identifiers

NCT01020253
YCU07-122

Details and patient eligibility

About

The purpose of this study is to evaluate whether alendronate and alfacalcidol are effective on prosthetic or lumbar spine BMD after total hip arthroplasty.

Enrollment

60 patients

Sex

All

Ages

44 to 82 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • osteoarthritis of the hip
  • patients after total hip arthroplasty

Exclusion criteria

  • diseases related to bone metabolism
  • patients taking drugs which affect bone metabolism

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 3 patient groups

Alendronate medication
Active Comparator group
Treatment:
Drug: alendronate, alfacalcidol
Alfacalcidol medication
Active Comparator group
Treatment:
Drug: alendronate, alfacalcidol
Non-medication
No Intervention group
Treatment:
Drug: alendronate, alfacalcidol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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