Serum Talin-1 and Cripto-1 in Colorectal Cancer
Talin-1/CR-1
Evaluating Serum Talin-1 and Cripto-1 as Diagnostic Biomarkers in Colorectal Cancer
1 other identifier
interventional
70
1 country
1
Brief Summary
The goals of this study are
- To evaluate the clinical utility of Talin-1 and Cripto-1 measurement in colorectal cancer patients in comparison with healthy controls.
- To Compare the diagnostic significance of serum Talin-1 and Cripto-1 with traditional serum biomarker CEA
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable colorectal-cancer
Started Mar 2026
Typical duration for not_applicable colorectal-cancer
1 active site
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
First Submitted
Initial submission to the registry
January 24, 2026
CompletedFirst Posted
Study publicly available on registry
February 17, 2026
CompletedStudy Start
First participant enrolled
March 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2029
February 17, 2026
January 1, 2026
2.8 years
January 24, 2026
February 12, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Serum Talin-1 measurement in colorectal cancer patients
measuring serum level of talin-1 in colorectal cancer patient to compare its level with healthy control
From enrollment up to one week
Secondary Outcomes (1)
Serum Cripto-1 measurement in colorectal cancer patients
From enrollment up to one week
Study Arms (1)
Group(1)
EXPERIMENTALInterventions
To evaluate the clinical utility of Talin-1 measurement in colorectal cancer patients in comparison with healthy controls.
To evaluate the clinical utility of Cripto-1 measurement in colorectal cancer patients in comparison with healthy controls.
Eligibility Criteria
You may qualify if:
- Age \>18 years Old.
- Patients of both sexes who met the clinical diagnostic criteria of colorectal cancer (change in bowel habit, absolute or recurrent constipation, rectal bleeding, significant weight loss or intestinal obstruction)
- Patients diagnosed with colorectal cancer by imaging and histopathology
You may not qualify if:
- Age \<18 years old.
- Patients with past history of chemotherapy or surgical excision of tumor
- Patients with familial adenomatous polyposis
- Patients with hereditary non-polyposis colorectal cancer
- Patients with inflammatory bowel disease
- patients with other types of tumors
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Assuit University Hospital
Asyut, Asyut Governorate, 17777, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant lecturer
Study Record Dates
First Submitted
January 24, 2026
First Posted
February 17, 2026
Study Start
March 30, 2026
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
December 31, 2029
Last Updated
February 17, 2026
Record last verified: 2026-01