Cervical Dysplasia Clinical Trials

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Cervical Cancer Detection Using Optical Spectroscopy

Who is this study for? Adult female patients with Early Stage Cervical Cancer that are undergoing colposcopy
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The objective of the work described in this protocol is to determine the optical signatures of cervical dysplasia using optical technologies.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

• undergoing colposcopy for the diagnosis of cervical cancer

• LEEP for the treatment of cervical cancer in early stages.

• Follow-up Pap smear in surveillance

Locations
United States
North Carolina
Duke University Medical Center
RECRUITING
Durham
Contact Information
Primary
Nimmi Ramanujam, Ph.D.
nimmi@duke.edu
919-660-5307
Time Frame
Start Date: 2006-05
Estimated Completion Date: 2028-01-31
Participants
Target number of participants: 350
Treatments
Experimental: Colposcope
Patients referred for GYN procedures. Specifically, patients will be referred for Pap smear, colposcope or LEEP. The intervention for this arm is the use of the bench-top, miniature optical spectrometer or trans-vaginal colposcope
Related Therapeutic Areas
Sponsors
Leads: Duke University

This content was sourced from clinicaltrials.gov