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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01262144
Other study ID # 421CTIL
Secondary ID
Status Completed
Phase N/A
First received November 23, 2010
Last updated December 15, 2010
Start date August 2010

Study information

Verified date November 2010
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Cervical Cancer is staged clinically, not surgically. Patients in whom an extensive disease is identified are not usually eligible for surgery. PET-CT is used to support staging. However, some patients received surgery after staging and subsequently require radio/chemotherapy due to findings on operation.

This study will attempt to find a correlation between SUV-Max on PET-CT and subsequent outcomes i.e. need for adjuvant therapy.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- having stating PET-CT stored on site

- treated with surgery

Exclusion Criteria:

- not eligible for surgery based on PET-CT, clinical stage

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Radiation:
Radiotherapy
Radiotherapy for cervical cancer

Locations

Country Name City State
Israel Rambam Medical Center City Haifa

Sponsors (1)

Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Administration of adjuvant therapy immediately following surgery No
Secondary Overall survival surgery - present day No
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