NCT06276309

Brief Summary

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2024

Geographic Reach
1 country

9 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2024

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

February 7, 2024

Completed
16 days until next milestone

First Posted

Study publicly available on registry

February 23, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2025

Completed
Last Updated

September 19, 2024

Status Verified

September 1, 2024

Enrollment Period

11 months

First QC Date

February 7, 2024

Last Update Submit

September 12, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • mortality rate

    3-year mortality rate for cervical neuroendocrine carcinoma

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

  • Disease-free survival

    3-year disease-free survival for cervical neuroendocrine carcinoma

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

Eligibility Criteria

Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All 300 patients were diagnosed with cervical neuroendocrine carcinoma by histopathology

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (9)

Fujian Maternity and Child Health Hospital

Fuzhou, Fujian, 350001, China

RECRUITING

Fujian Provincial Hospital

Fuzhou, Fujian, China

RECRUITING

Ningde Mindong Hospital

Ningde, Fujian, China

RECRUITING

Putian City first Hospital

Putian, Fujian, China

RECRUITING

The Second Affiliated Hospital of Fujian Medical University

Quanzhou, Fujian, China

RECRUITING

Zhangzhou affiliated Hospital of Fujian Medical University

Zhangzhou, Fujian, 363000, China

RECRUITING

Maternal and Child Health Hospital of Hubei Province

Wuhan, Hubei, China

RECRUITING

Xiangya Hospital, Central South University

Changsha, Hunan, China

RECRUITING

Jiangxi maternal and Child Health Hospital

Nanchang, Jiangxi, China

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

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.

MeSH Terms

Conditions

Neuroendocrine TumorsUterine Cervical Neoplasms

Condition Hierarchy (Ancestors)

Neuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasmsNeoplasms, Nerve TissueUterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by SiteUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Diseases

Study Officials

  • Pengming Sun, PhD

    Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 7, 2024

First Posted

February 23, 2024

Study Start

February 1, 2024

Primary Completion

December 30, 2024

Study Completion

February 28, 2025

Last Updated

September 19, 2024

Record last verified: 2024-09

Locations