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NCT Number: NCT06276309

Protein Molecular Characteristics and Prognosis of Cervical Neuroendocrine Tumors

The clinical diagnosis and treatment data of 300 cases of cervical neuroendocrine tumors were collected, including age, preoperative biopsy pathology results, postoperative histopathological results, TCT results, and colposcopy biopsy pathology results. At the same time, paraffin tissue specimens (remaining specimens after pathological diagnosis) from 100 cases of cervical neuroendocrine tumors from multiple centers across the country were collected to establish a cervical neuroendocrine tumor data follow-up database. Protein concentration and omics analysis were performed on the data results, to evaluate the molecular characteristics and prognosis of cervical neuroendocrine tumor proteins, and to preliminarily explore its clinical application value.

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Key information

About this study

  • The clinical diagnosis and treatment data of 300 cases of cervical neuroendocrine tumors were used for prognostic analysis.

(1) The diagnosis and treatment information of cervical neuroendocrine carcinoma in multiple hospitals was collected, including clinical and medical data such as age, preoperative HPV genotyping, preoperative biopsy pathological results, postoperative histopathological results, FIGO staging, prognosis and survival information, and follow-up of patients.

  • Protein and other omics analysis was performed on paraffin tissues of 100 cases of cervical neuroendocrine tumors Paraffin samples collected from 100 cases of cervical neuroendocrine tumors were identified, processed and segmtioned, and protein concentration and proteome were determined to establish the molecular characteristics and prognostic targets of cervical neuroendocrine tumors.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients diagnosed with cervical neuroendocrine carcinoma by histopathology
  • Clinical data were complete

Exclusion criteria

  • Patients who are not being treated in our hospital
  • Patients with lack of follow-up data, unable to obtain survival information
  • Patients call to refuse to participate in this project
  • The quality of paraffin specimens can not meet the requirements of proteome concentration determination

Treatment and study plan

Primary outcomes

  1. mortality rate

    Time frame: Among patients with cervical neuroendocrine carcinoma, the mortality rate within 3 years following surgery

    3-year mortality rate for cervical neuroendocrine carcinoma

  2. Disease-free survival

    Time frame: Among patients with cervical neuroendocrine carcinoma, the disease-free survival within 3 years following surgery

    3-year disease-free survival for cervical neuroendocrine carcinoma

Study contacts

Contact information is provided by the study sponsor or research team.

Binhua Dong

CONTACT

[email protected]

+86-0591-87558732

Pengming Sun

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Fujian Maternity and Child Health Hospital

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Feb 23, 2024
Registry last updated
Sep 19, 2024

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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