NCT05426135

Brief Summary

To improve the accuracy of risk prediction, screening and treatment outcome of cancer, we aim to establish a medical database that includes standardized and structured clinical diagnosis and treatment information, image features, pathological features, and multi-omics information and to develop a multi-modal data fusion-based technology system using artificial intelligence technology based on database.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
3,000

participants targeted

Target at P75+ for all trials

Timeline
5mo left

Started Jun 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

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 Progress91%
Jun 2022Oct 2026

Study Start

First participant enrolled

June 1, 2022

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

June 15, 2022

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 21, 2022

Completed
3.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Expected
Last Updated

June 21, 2022

Status Verified

June 1, 2022

Enrollment Period

3.3 years

First QC Date

June 15, 2022

Last Update Submit

June 17, 2022

Conditions

Outcome Measures

Primary Outcomes (4)

  • The outcome of clinical diagnosis of suspected patients with lung cancer/pulmonary nodular (Benign/Malignant nodule)

    The outcome of clinical diagnosis of patients with lung cancer/pulmonary nodular (Benign/Malignant nodule). ① Benign nodule ② Malignant neoplasm/nodule: squamous cell carcinoma, adenocarcinoma, small cell carcinoma, and large cell carcinoma.

    2022-2026

  • The outcome of clinical diagnosis of suspected patients with stomach cancer or lesion (Benign/Malignant).

    ① Benign ② Malignant

    2022-2026

  • The outcome of clinical diagnosis of suspected patients with colorectal cancer or lesion (Benign/Malignant).

    ① Benign ② Malignant

    2022-2026

  • Treatment response of anti-cancer therapy at first evaluation in patients with lung/stomach/colorectal cancer (CR, PR, PD, SD).

    The treatment response of anti-cancer therapy at first evaluation in patients with lung/stomach/colorectal cancer follows The Response Evaluation Criteria In Solid Tumors (RECIST version 1.1) from the World Health Organization (WHO). The evaluation index is as follows. CR (complete response): Disappearance of all target lesions and reduction in the short axis measurement of all pathologic lymph nodes to ≤10 mm. PR (partial response): 30% decrease in the sum of the longest diameter of the target lesions compared with baseline. PD (progressive disease):≥20% increase of at least 5 mm in the sum of the longest diameter of the target lesions compared with the smallest sum of the longest diameter recorded OR The appearance of new lesions, including those detected by FDG-PET (fludeoxyglucose positron emission tomography). SD (stable disease): Neither PR nor PD.

    2022-2026

Study Arms (3)

Lung cancer group

Participants with lung cancer/pulmonary nodules

Stomach cancer group

Participants with Stomach cancer/Stomach lesion

Colorectal cancer group

Participants with Colorectal cancer/Colorectal lesion

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients the suspected of lung cancer/node, or stomach cancer/lesion, or colorectal cancer/leision

You may qualify if:

  • Participants with the suspected of lung cancer/node, or stomach cancer/lesion, or colorectal cancer/leision
  • Participants that have signed informed consent.
  • Participants with detailed electronic medical records, image records, pathological records, multi-omics information, and other important clinical diagnostic information.
  • Healthy participants with no clinical diagnosis of lung cancer/node, or stomach cancer/lesion, or colorectal cancer/leision.

You may not qualify if:

  • Participants with primary clinical and pathological data missing.
  • Participants lost to follow-up.
  • Participants with too poor medical image quality to perform segment and mark ROI accurately

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, 430000, China

RECRUITING

MeSH Terms

Conditions

Lung NeoplasmsStomach NeoplasmsColonic NeoplasmsNeoplasms, Second Primary

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract DiseasesGastrointestinal NeoplasmsDigestive System NeoplasmsDigestive System DiseasesGastrointestinal DiseasesStomach DiseasesColorectal NeoplasmsIntestinal NeoplasmsColonic DiseasesIntestinal Diseases

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 15, 2022

First Posted

June 21, 2022

Study Start

June 1, 2022

Primary Completion

October 1, 2025

Study Completion (Estimated)

October 1, 2026

Last Updated

June 21, 2022

Record last verified: 2022-06

Locations