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NCT06254729: EECC

Clinical Study on the Evaluation of the Efficacy of Cervical Cancer

Not yet recruiting Last updated 12 February 2024
What this trial tests

trial testing Observational study in Uterine Cervical Neoplasms in 4,000 participants. Not yet recruiting.

Timeline
16 February 2024
Primary endpoint
16 February 2029
16 February 2030

Quick facts

Lead sponsorFirst Affiliated Hospital Xi'an Jiaotong University
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment4,000
Start date16 February 2024
Primary completion16 February 2029
Estimated completion16 February 2030

Drugs / interventions tested

Conditions studied

Sponsor

First Affiliated Hospital Xi'an Jiaotong University

Who can join

18 and older, female only, with Uterine Cervical Neoplasms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main objectives of this study are to construct a multi-omics-based prognostic and side-effect prediction model for cervical cancer based on pre-treatment imaging, digital pathology, genomics, proteomics, molecular biology, metabolomics, and intestinal flora characteristics data of cervical cancer patients, combined with patients' clinical information, to guide the precise treatment of cervical cancer patients; and to deeply excavate the characteristics related to recurrent cervical cancer based on time-series multi-omics data. Construct an artificial intelligence auxiliary model for dynamic monitoring of cervical cancer recurrence based on longitudinal multi-omics. To provide a real-time and timely tool for clinical early prediction, early identification, early diagnosis and early intervention of cervical cancer, to prolong the survival time and improve the quality of patients' survival. 1. To realize multi-omics feature extraction of cervical cancer patients before treatment, and build a prognosis and side-effect prediction model of cervical cancer to guide accurate treatment; 2. To make iterative, comprehensive, real-time assessment of the risk of recurrence of cervical cancer based on time-series multi-omics data, and to build an early warning model for early identification and early diagnosis of recurrent cervical cancer; 3. To establish a prognostic and side-effect prediction and risk dynamic assessment model for cervical cancer, to build an intelligent decision support system, to implement the application of prognostic and side-effect prediction and dynamic monitoring model, to further assist in the precise diagnosis and treatment of cervical cancer, and to provide an accurate prognostic tool for identifying, diagnosing, and intervening in cervical cancer during the follow-up process.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Observational study

Trials testing the same drug.

Other recruiting trials for Uterine Cervical Neoplasms

Currently open trials in the same condition.

Other First Affiliated Hospital Xi'an Jiaotong University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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