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NCT01008540: PHRC CMV
Cytomegalovirus Resistance in Transplant Patients and Bone Marrow Recipients in the Prophylaxis Era, a French Multicentric Cohort Study
NA trial testing depistage in Cytomegalovirus in 800 participants. Completed in 1 June 2012.
1 December 2010
Quick facts
| Lead sponsor | University Hospital, Limoges |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 800 |
| Start date | 1 August 2006 |
| Primary completion | 1 December 2010 |
| Estimated completion | 1 June 2012 |
| Sites | 33 locations across France |
Drugs / interventions tested
- depistage — full drug profile →
Conditions studied
- Cytomegalovirus — all drugs for Cytomegalovirus →
Sponsor
University Hospital, Limoges
Who can join
Eligibility, any sex, with Cytomegalovirus. 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.
- Resistance incidence in our patients with subgroup analysis, by organ and by the use of prophylaxis or preemptive treatment
Sponsor's own description
The investigators aim is to determine the incidence of cytomegalovirus resistance to antivirals in a cohort study. The patients are included at their first CMV active infection and are followed during two years thereafter. When criteria for suspected resistance are meet, blood and urine samples are collected for virus isolation and further resistance phenotype, and for resistance genotype determination. Results are compared with baseline samples. Clinical information such as treatment, immunosuppressive regimen and clinical evolution will be collected. Through this study, the investigators aim to organize a national network for the detection and identification of CMV resistant strains that will be useful when new therapeutics will be available.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Drug-resistant cytomegalovirus in transplant recipients: a French cohort study.
Hantz S, Garnier-Geoffroy F, Mazeron MC, Garrigue I, et al · · 2010 · cited 109× · PMID 20961907 · DOI 10.1093/jac/dkq368
Verify or expand the search:
- PubMed search for NCT01008540
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Cytomegalovirus
Currently open trials in the same condition.
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- NCT06958796 — Strategic Help With Immunoglobulin to Enhance Protect Against Late Disease (CMV) · Phase 4 · recruiting
- NCT05664126 — Haplo-identical Viral-Specific T-cells for Treatment of Cytomegalovirus and Adenovirus Infections After Hematopoietic Ce · Phase 2 · recruiting
- NCT05575492 — A Study of mRNA-1647 Cytomegalovirus Vaccine in Healthy Participants 9 to 15 Years of Age and Participants 16 to 25 Year · Phase 1, PHASE2 · active not recruiting
- NCT03665675 — Donor Virus-Specific CMV or AdV CTL to Treat CMV or AdV Reactivation or Disease After Solid Organ or HCT · EARLY_PHASE1 · recruiting
Other University Hospital, Limoges 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)
- Trial protocol + status: ClinicalTrials.gov NCT01008540 (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, Limoges
- Last refreshed: 17 July 2025
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/NCT01008540.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing