Clinical trial • Musculoskeletal

Zoledronic acid for Hip osteoarthritis

Clinical trial of Zoledronic acid for Hip osteoarthritis. Randomised, placebo (dose/schedule not specified)-controlled. 70 participants.

Overview

Trial Therapeutic Area
Musculoskeletal
Trial Disease
Hip osteoarthritis
Drug Modality
Small molecule

Key dates

Initial CTIS Submission Date
28-04-2025
First CTIS Authorization Date
15-05-2025

Trial design

Randomised, placebo (dose/schedule not specified)-controlled trial in Norway.

Randomised
Yes
Comparator
Placebo (dose/schedule not specified)
Target Sample Size
70

Eligibility

Recruits 70 No vulnerable populations selected (isVulnerablePopulationSelected:false). Consent/assent handling not specified..

Vulnerable Population
No vulnerable populations selected (isVulnerablePopulationSelected:false). Consent/assent handling not specified.

Recruitment

Planned Sample Size
70
Recruitment Window Months
14

Geography

Total Number Of Sites
1
Total Number Of Participants
70

Norway

Earliest CTIS Part Ii Submission Date
25-04-2025
Latest Decision Or Authorization Date
15-05-2025
Processing Time Days
20
Number Of Sites
1
Number Of Participants
70

Sites

Site Name
Martina Hansens Hospital AS
Department Name
Orthopedic
Principal Investigator Name
Morten Halkjær Iversen
Principal Investigator Email
Morten.Halkjaer.Iversen@mhh.no
Contact Person Name
Morten Halkjær Iversen
Contact Person Email
Morten.Halkjaer.Iversen@mhh.no

Sponsor

Primary sponsor

Full Name
Martina Hansens Hospital AS
Organisation Type
Hospital/Clinic/Other health care facility
Country Of Registered Address
Norway

Investigational products

Investigational Product Name
Zoledronic Acid
Active Substance
Zoledronic acid
Modality
Small molecule

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