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OpenTrials
Completed

NCT Number: NCT01262144

SUV Max as Predictor of Outcome in Cervical Cancer

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • having stating PET-CT stored on site
  • treated with surgery

Exclusion criteria

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

Treatment and study plan

Radiotherapy

Radiation

Radiotherapy for cervical cancer

Primary outcomes

  1. Administration of adjuvant therapy

    Time frame: immediately following surgery

Secondary outcomes

  1. Overall survival

    Time frame: surgery - present day

Sponsors and collaborators

Lead sponsor

Rambam Health Care Campus

Other

Registry information

Official study title

A Study to Evaluate the Value of SUV-Max in PET-FDG in Predicting Outcome of Surgery Vis a Vis Need for Radiotherapy

Important dates

Study start
2010
First posted
Dec 17, 2010
Registry last updated
Dec 17, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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