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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01562067
Other study ID # 125-11CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 21, 2012
Last updated March 22, 2012
Start date March 2012
Est. completion date April 2014

Study information

Verified date March 2011
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 tumors are characterized by vascular changes (in terms of quantity, volume and Flows) in the tumor. Due to a good access to the cervix through the vagina, these parameters can be assessed using a three dimensional supersonic. Sonographic characteristics of tumor indices measures before and after oncological treatments may shed light on the patient's prognosis.


Description:

no editional information. see above


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date April 2014
Est. primary completion date April 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Cervical cancer patients intended to undergo chemotherapy or radiation, or both

Exclusion Criteria:

- no exclusions

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
ultrasound examination
ultrasound and doppler studies to evaluate size and vascularity of tumor during radiotherapy

Locations

Country Name City State
Israel Rambam Medical Center 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 Sonographic characteristics of cervical tumors Sonographic characteristics of cervical tumors indices measures before and after oncological treatments may shed light on the patient's prognosis. 5 years No
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