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NCT06556953Completed

Evaluating the Risk of Postoperative Venous Thromboembolism in Cervical Cancer Patients

Development and Validation of Machine Learning Models to Evaluate the Postoperative Venous Thromboembolism Risk of Cervical Cancer Patients in China

Source: ClinicalTrials.gov · Last updated 16 Aug 2024

Brief summary (registry, in English)

The aim of this study is to develop a machine learning model to accurately predict the risk of venous thromboembolism in patients with cervical cancer after surgery.

Status (registry)
Completed
Study type
Observational
Enrollment
1174 (actual)
First submitted
6 Aug 2024
Start date
1 Jan 2019
Primary completion date
31 Dec 2023
Lead sponsor
Haike Lei
NCT number
NCT06556953

What you commit to

  • Study type: Observational
  • Participants enrolled: 1174
  • From 1 Jan 2019 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of VTE caused by other reasons before surgery.
  • Secondary cervical cancer or accompanying primary malignant tumor.

Age

  • Patients under the age of 18.

Who the study is looking for

  • Confirmation of cervical cancer through pathological examination.
  • Receipt of surgical treatment for cervical cancer at Chongqing University Cancer Hospital in China.
  • Provision of comprehensive case information.

Age in the registry: 20 years to 89 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chongqing University Cancer Hospital
Coordinator of this site? Confirm its status
ChongqingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.