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Dual mechanism study to explore the novel circular RNA circ_0001642 promoting colorectal cancer progression based on multi-omics technology

Dual mechanism study to explore the novel circular RNA circ_0001642 promoting colorectal cancer progression based on multi-omics technology

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098024
Enrollment
Unknown
Registered
2025-02-28
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal cancer

Interventions

Observation Group:None
Control group:None

Sponsors

Yantai Affiliated Hospital of Binzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age >=18 years, confirmed diagnosis of colorectal adenocarcinoma (based on postoperative pathology or biopsy pathology), clinical stage I-IV; 2) Prospective study (2025.01-2027.12) requires signed informed consent and voluntary provision of tumor tissue, paracancerous tissue and peripheral blood samples; 3) Retrospective cohort (2019.01-2023.12) requires complete clinical data and follow-up records (including date of diagnosis, treatment regimen, survival status, etc.); 4) Have not received radiotherapy or targeted therapy (preoperative neoadjuvant therapy patients can be included); 5) Can cooperate to complete long-term follow-up (for retrospective analysis).

Exclusion criteria

Exclusion criteria: 1) comorbidity with other malignant tumors or systemic immune disorders; 2) Presence of severe hepatic or renal insufficiency, cardiovascular or cerebrovascular disease or other comorbidities that may affect the survival analysis; 3) Missing clinical information or incomplete follow-up data (e.g., missed visits, incorrect contact information, etc.); 4) Pathological type of non-adenocarcinoma (e.g. neuroendocrine tumor, lymphoma, etc.); 5) hemolysis or substandard tissue preservation during sample collection (for prospective studies only).

Design outcomes

Primary

MeasureTime frame
The expression level of SPHK1;The expression level of hsa_circ_0001642;The expression level of hsa-miR-193a-5p;Survival outcome indicators;Diagnostic effectiveness indicators;

Secondary

MeasureTime frame
Correlation of clinicopathologic parameters;Patient quality of life scores;

Countries

China

Contacts

Public ContactYandong Miao

Yantai Affiliated Hospital of Binzhou Medical University

miaoyd_22@bzmc.edu.cn+86 182 9881 0814

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026