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NCT00372281
Comparison of Cliavist Enhancement in Infectious and Degenerative Diseases of the Spine
Phase 3 trial testing Cliavist in Spine Infection in 40 participants. Status unknown.
1 August 2009
Quick facts
| Lead sponsor | University Hospital, Strasbourg, France |
|---|---|
| Phase | Phase 3 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 40 |
| Start date | 1 March 2007 |
| Primary completion | 1 August 2009 |
| Estimated completion | 1 December 2009 |
| Sites | 4 locations across France |
Drugs / interventions tested
- Cliavist — full drug profile →
Conditions studied
- Spine Infection — all drugs for Spine Infection →
Sponsor
University Hospital, Strasbourg, France
Who can join
18 and older, any sex, with Spine Infection. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
First MRI: performed immediately after gadolinium administration
Time frame: immediately after gadolinium administration -
Second MRI: performed 24 hours after cliavist administration
Time frame: 24 hours after cliavist administration
Sponsor's own description
USPIO contrast enhancement results from intracellular trapping of the iron particles in reactive cells, especially macrophages. 17FDG-PET studies have demonstrated that macrophages are present in spine infectious diseases but are absent in spine degenerative diseases. The aim of this work is to compare the enhancement induced by CLIAVIST in both diseases. The absence of macrophages in degenerative lesions should help to differentiate them from infectious lesions, who should present contrast enhancement in relation to the presence of macrophages.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Advances in magnetic nanoparticles for molecular medicine.
Yang X, Kubican SE, Yi Z, Tong S. · · 2025 · cited 8× · PMID 39846549 · DOI 10.1039/d4cc05167j
Verify or expand the search:
- PubMed search for NCT00372281
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Spine Infection
Currently open trials in the same condition.
- NCT06284174 — Effectiveness of Povidone-Iodine Versus Chlorhexidine Gluconate Solutions in Reducing Microbial Contamination in Spinal · NA · recruiting
Other University Hospital, Strasbourg, France trials
Trials by the same sponsor.
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- NCT07302646 — Optimizing Reduced-Flow, Low-Volume Contrast Protocols for Cerebral Angiography in Unruptured Aneurysms · NA · not yet recruiting
- NCT07273968 — Clinical Study Evaluating the Effect of Virtual Reality on Reducing Patients' Anxiety During Wisdom Teeth Extraction · NA · not yet recruiting
- NCT07214103 — Phase IIb Multicenter Randomized Controlled Trial Evaluating the Efficacy of Sivelestat in Patients With Septic Coagulop · Phase 2 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00372281 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University Hospital, Strasbourg, France
- Last refreshed: 24 February 2009
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/NCT00372281.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing