Skip to content

FLT F-18 PET/CT in diagnosis, staging and terapy assessmentin tumours with accelereted replication

FLT F-18 PET/CT in diagnosis, staging and terapy assessmentin tumours with accelereted replication - FLT F-18 PET/CT in tumours

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2012-002820-33-IT
Enrollment
100
Registered
2012-10-25
Start date
2013-06-26
Completion date
Unknown
Last updated
2013-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients complying with cancer for whom is mandatory to know the replicative cellular activty MedDRA version: 14.1 Level: SOC Classification code 10022891 Term: Investigations System Organ Class: 10022891 - Investigations MedDRA version: 14.1 Level: SOC Classification code 10029104 Term: Neoplasms benign, malignant and unspecified (incl cysts and polyps) System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)

Interventions

Product Name: F18 FLT Product Code: NA Pharmaceutical Form: Radiopharmaceutical precursor Other descriptive name: FLT F18 Concentration unit: MBq megabecquerel(s) Concentration type: equal Concentrati

Sponsors

CENTRO DI RIFERIMENTO ONCOLOGICO DI BASILICATA
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients for whom is mandatory to know cellular replication and to monitor therpy efficacy early Are the trial subjects under 18? no Number of subjects for this age range: 0 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 70 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 30

Exclusion criteria

Exclusion criteria: • Age 90 yrs

Design outcomes

Primary

MeasureTime frame
Main Objective: Impact of F18 FLT PET/CT for replicative evaluation in staging, restaging and therapy assessment of tumours rather than energetic metabolism;Secondary Objective: correlation to angiogenetic markers and EGFR mutations;Primary end point(s): Diagnostic accuracy of F18 FLT PET/CT;Timepoint(s) of evaluation of this end point: 48 months

Secondary

MeasureTime frame
Secondary end point(s): metastatic assessment and correlation to neoplastic markers;Timepoint(s) of evaluation of this end point: 48 months

Countries

Italy

Contacts

Public ContactMedicina Nucleare

IRCCS CROB centro di riferimento oncologico di basilicata

giosto24@hotmail.com0972-726560

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026