FLT-PET for Early Detection of Relapse in Patients With Irradiated Lung Cancer

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Completed
CT.gov ID
NCT02995889
Collaborator
(none)
64
2
1
63.2
32
0.5

Study Details

Study Description

Brief Summary

This study investigates the feasibility of FLT-PET to improve the diagnosis of relapse in patients with irradiated lung cancer in comparison with FDG-PET/CT.

Condition or Disease Intervention/Treatment Phase
  • Device: FLT-PET
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
FLT-PET for Early Detection of Relapse in Patients With Irradiated Lung Cancer
Study Start Date :
Nov 1, 2014
Actual Primary Completion Date :
Feb 7, 2019
Actual Study Completion Date :
Feb 7, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: FLT-PET

Device: FLT-PET

Outcome Measures

Primary Outcome Measures

  1. Number of patients with local and/or regional relapse [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • history with lung cancer, small cell or non-small cell

  • radiotherapy of lung cancer ended within the last 24 months

  • radiotherapy might be normofractionated or stereotactic

  • current suspicion of relapse

  • written and oral consent

Exclusion Criteria:
  • communication difficulties

  • pregnancy or lactation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dept. of Clinical Physiology, Nuclear Medicine and PET, Rigshospitalet Copenhagen Denmark 2100
2 Dept. Respiratory Medicine, Bispebjerg University Hospital Copenhagen Denmark 2400

Sponsors and Collaborators

  • Rigshospitalet, Denmark

Investigators

  • Study Chair: Andreas Kjær, MD phD MDSci, Dept of Clinical Physiology, Nuclear medicine and PET, Rigshospitalet, Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tine Nøhr Christensen, MD, research fellow, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT02995889
Other Study ID Numbers:
  • 308_14
First Posted:
Dec 19, 2016
Last Update Posted:
May 9, 2022
Last Verified:
May 1, 2022

Study Results

No Results Posted as of May 9, 2022