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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04868097
Other study ID # 0186-20-KMC
Secondary ID 0186-20-KMC
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date March 31, 2023

Study information

Verified date April 2021
Source Kaplan Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A pre- operative evaluation for the presence of intermediate risk factors prior to surgery may allow for better patient counselling, modify the course of surgery or select patients to undergo primary chemo- radiation. The purpose of this study is to validate that the presence of histological risk factors in a pre-operative large loop biopsy highly correlates with post-operative histological evaluation and the subsequent indication for post-operative chemo-radiation


Description:

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Study Design


Intervention

Procedure:
cervix biopsy
large loop electrosurgical cervix biopsy

Locations

Country Name City State
Israel Kaplan Medical Center Re?ovot

Sponsors (3)

Lead Sponsor Collaborator
Kaplan Medical Center Barzilai Medical Center, Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary The rate of LVSI in Cervix cancer Pre operative presence of LVSI in loop biopsy in cervical cancer, compared to post operative LVSI rate in hysterectomy Specimen two years
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