NCT00791609

Brief Summary

Feasibility of accurate differentiation between malignant and benign tissue using the FOSTI device on surgically removed tissue

Trial Health

50
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2008

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

November 13, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 14, 2008

Completed
Last Updated

November 14, 2008

Status Verified

November 1, 2008

First QC Date

November 13, 2008

Last Update Submit

November 13, 2008

Conditions

Cancer

Keywords

cancer

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population will consist of subjects who undergo cancer surgery

You may qualify if:

  • Subjects of all ages.
  • Subject is able, agree and sign the Informed Consent Form.

You may not qualify if:

  • Subject has any conditions, which precludes compliance with study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neoplasms

Study Officials

  • Anatoliy Babchenko

    Optivasive Ltd.

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
INDUSTRY

Study Record Dates

First Submitted

November 13, 2008

First Posted

November 14, 2008

Study Start

March 1, 2008

Last Updated

November 14, 2008

Record last verified: 2008-11