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Phase I Study of HAL Formulations Applied to the Cervix in Healthy Volunteers

This study has been terminated.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00496171
First Posted: July 4, 2007
Last Update Posted: January 16, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
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July 3, 2007
July 4, 2007
January 16, 2009
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Complete list of historical versions of study NCT00496171 on ClinicalTrials.gov Archive Site
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Phase I Study of HAL Formulations Applied to the Cervix in Healthy Volunteers
A Phase I Hexaminolevulinate (HAL) Dose-Finding Study Applying Different Formulations to the Cervix in Healthy Volunteers
The purpose of the study is to determine the most effective formulation of HAL for release of hexaminolevulinate to the cervical epithelium at different doses.
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Observational
Time Perspective: Prospective
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Healthy
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
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Inclusion Criteria:

  • Healthy, pre-menopausal female volunteers

Exclusion Criteria:

  • Acute or chronic disease which could influence the study results
Sexes Eligible for Study: Female
18 Years and older   (Adult, Senior)
Yes
Contact information is only displayed when the study is recruiting subjects
Norway
 
 
NCT00496171
PC CE102/07
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Photocure
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Principal Investigator: Claes G Tropé, MD PhD Riks-Radium University Hospital
Photocure
January 2009