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PET-CT Scan as a Diagnostic Method in Unknown Primary Tumors
This study is currently recruiting participants.
Verified by Rigshospitalet, Denmark, May 2008
Sponsored by: Rigshospitalet, Denmark
Information provided by: Rigshospitalet, Denmark
ClinicalTrials.gov Identifier: NCT00269373
  Purpose

Is PET-CT scan better than PET or CT alone in diagnosing primary tumours in patients with unknown primary tumors? Can information obtained with PET-CT replace other clinical and radiological investigations? Is PET/CT cost-effective?


Condition Intervention
Unknown Primary Tumor
Procedure: PET-CT

MedlinePlus related topics: CT Scans Cancer Nuclear Scans
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: PET-CT Scan as a Diagnostic Method in Unknown Primary Tumors

Further study details as provided by Rigshospitalet, Denmark:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 136
Study Start Date: December 2005
Estimated Study Completion Date: December 2008
Intervention Details:
    Procedure: PET-CT
    no drugs included
Detailed Description:

Patients who fulfill the international definition of unknown primary tumors can be included, except:

  • Young men (<55 years) with growing mid-line tumors where a germ cell tumor could be expected will not be included.
  • Patients with lymph-node metastases with squamous cell carcinoma in the head and neck region will not be included.
  • Women with adenocarcinoma in lymph nodes in the axilla will not be included.
  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients with unknown tumors

Criteria

Inclusion Criteria:

  • Unknown primary tumors

Exclusion Criteria:

  • Young men (<55 years) with growing mid-line tumors where a germ cell tumor could be expected will not be included.
  • Patients with lymph-node metastases with squamous cell carcinoma in the head and neck region will not be included
  • Women with adenocarcinoma in lymph nodes in the axilla will not be included
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00269373

Contacts
Contact: Gedske Daugaard, MD 45-35-454-677 gedske.daugaard@rh.regionh.dk

Locations
Denmark
Rigshospitalet Recruiting
Copenhagen, Denmark, 2100
Principal Investigator: Gedske Daugaard, MD            
Sponsors and Collaborators
Rigshospitalet, Denmark
Investigators
Principal Investigator: Gedske Daugaard Rigshospitalet, Denmark
  More Information

Responsible Party: Rigshospitalet ( Gedske Daugaard )
Study ID Numbers: 01 283694
Study First Received: December 22, 2005
Last Updated: May 20, 2008
ClinicalTrials.gov Identifier: NCT00269373  
Health Authority: Denmark: Ethics Committee

Keywords provided by Rigshospitalet, Denmark:
Unknown primary tumor
PET-CT

Study placed in the following topic categories:
Neoplasms, Unknown Primary
Neoplasm Metastasis

Additional relevant MeSH terms:
Neoplasms
Neoplastic Processes
Pathologic Processes

ClinicalTrials.gov processed this record on January 16, 2009