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Clinical Trials/NCT00250055
NCT00250055
Terminated
Not Applicable

Non-Invasive, Real-time Technology for Diagnosis of Cervical Tissue

University of New Mexico1 site in 1 country100 target enrollmentApril 2004
ConditionsCervixCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervix
Sponsor
University of New Mexico
Enrollment
100
Locations
1
Primary Endpoint
The objective of this study is to determine whether non-invasive measurements of light transport through tissue can identify pre-cancerous and cancerous conditions.
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

In general, to determine the sensitivity of light transport to tissue from morphological features of clinical significance.

Determine how specific structural features contribute to light scattering. Investigate light scattering differences in tumorigenic and nontumorigenic cells.

Develop and implement quantitative and sensitive methods for measuring morphological properties.

Clinical measurements.

Detailed Description

Patients undergoing a colposcopy will also have spectroscopy measurements taken and an extra biopsy of suspicious tissue.

Registry
clinicaltrials.gov
Start Date
April 2004
End Date
January 2010
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with abnormal Pap smears who are referred for colposcopy.
  • Exclusion criteria include:
  • Anyone of the male sex since this study focuses on cervical cell abnormalities
  • Any woman who has had a hysterectomy, LEEP, or chemotherapy.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

The objective of this study is to determine whether non-invasive measurements of light transport through tissue can identify pre-cancerous and cancerous conditions.

Time Frame: 6 years

Study Sites (1)

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