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Clinical Trials/EUCTR2007-004393-81-AT
EUCTR2007-004393-81-AT
Active, not recruiting
Phase 1

Prospektive Evaluation von Multimodality Imaging Verfahren (PET - CT - MRT - US - Bildfusion) bei malignen Tumoren der Kopf-Hals-Region

Medizinische Universität Innsbruck - Universitätsklinik für Radiodiagnostik (Radiologie I)0 sites270 target enrollmentApril 1, 2008

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Patients with malignant Head and Neck Tumors - Diagnostic Imaging Study
Sponsor
Medizinische Universität Innsbruck - Universitätsklinik für Radiodiagnostik (Radiologie I)
Enrollment
270
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 1, 2008
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Medizinische Universität Innsbruck - Universitätsklinik für Radiodiagnostik (Radiologie I)

Eligibility Criteria

Inclusion Criteria

  • ?Patienten, die mit einem de\-novo\-Kopf\-Hals\-Tumor auf der HNO\-Klinik vorgestellt werden und klinisch schlüssige Hinweise auf einen malignen Tumor haben.
  • ?Patienten mit klinischem Verdacht auf ein Rezidiv eines Kopf\-Hals\-Tumors.
  • ?Mindestalter 18 Jahre
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • ?Eingriffe im Kopf\-Hals\-Bereich innerhalb von 3 Monaten vor der Bildgebung
  • ?Renale Retention mit Kreatininwert \> 1,5 mg/dl (Patienten mit oraler Diabeteseinstellung mit Metformin bei werden bei einem Serumkratininwert \< 1,5 mg/dl und entsprechender Hydrierung laut Guidelines der European Society of Urogenital Radiology eingeschlossen).
  • ?Bekannte Allergie auf jodhältige Kontrastmittel
  • ?Hyperthyreose
  • ?Implantierte elektronische Devices ohne MRT\-Freigabe
  • ?Klaustrophobie
  • ?Gravidität
  • ?Fehlendes Einverständnis zur Teilnahme an der Studie
  • ?Fehlende Geschäftsfähigkeit

Outcomes

Primary Outcomes

Not specified

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