NCT06324708 (THA_DXA) is a NA clinical trial of DXA in Bone Resorption, sponsored by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio.

Who is sponsoring NCT06324708?

NCT06324708 is sponsored by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio.

What drugs are being tested in NCT06324708?

Interventions in NCT06324708: DXA.

What condition does NCT06324708 study?

NCT06324708 studies Bone Resorption, Arthroplasty Complications.

Is NCT06324708 still recruiting?

NCT06324708 is currently status unknown. Last updated 22 March 2024.

Last reviewed 2024-03-22 · How we verify

NCT06324708: THA_DXA

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Analysis of Defined Elements on DXA in Patients Undergoing Hip Arthroplasty

Status unknown NA Last updated 22 March 2024

What this trial tests

NA trial testing DXA in Bone Resorption in 69 participants. Status unknown.

Timeline

7 February 2023

Primary endpoint
31 October 2024

31 October 2025

Quick facts

Lead sponsor	I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Phase	NA
Status	Status unknown
Study type	INTERVENTIONAL
Allocation	na
Design	single group
Masking	none
Primary purpose	diagnostic
Enrollment	69
Start date	7 February 2023
Primary completion	31 October 2024
Estimated completion	31 October 2025
Sites	1 location across Italy

Drugs / interventions tested

Conditions studied

Bone Resorption — all drugs for Bone Resorption →
Arthroplasty Complications — all drugs for Arthroplasty Complications →

Sponsor

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio — full company profile →

Who can join

Adults 50 to 90, any sex, with Bone Resorption or Arthroplasty Complications. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to investigate the role of two-dimensional FEM models obtained from DXA images in the longitudinal assessment of periprosthetic bone, in subjects undergoing hip arthroplasty. Specifically, the study will focus on the joint analysis of changes in the parameters of bone mineral density (BMD) and Bone Strain Index (BSI) at the level of periprosthetic bone of the proximal femur in patients undergoing hip replacement surgery using DXA, evaluating the densitometric variation of these two parameters over time, starting from an immediately postoperative data and checking the change at 6 months to follow the patient through the postoperative course

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

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Currently open trials in the same condition.

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Other I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio trials

Trials by the same sponsor.

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Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT06324708 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Last refreshed: 22 March 2024

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06324708.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing