- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07414082
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
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
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Colorectal cancer (CRC) is a major global health concern, ranking as the third most commonly diagnosed cancer and the second leading cause of cancer-related deaths. CRC is a malignancy predominantly affecting older adults, posing significant threats to their health and creating formidable challenges for healthcare systems.
Compared to younger patients, elderly CRC often presents with atypical symptoms. In some cases, the initial manifestations are not hematochezia or abdominal pain but anaemia and weight loss, leading to frequent late-stage (Stage IV) diagnoses, which complicates treatment.
Talin-1 serves as a crucial element within the multiprotein adhesion complexes that facilitate processes such as cell migration, adhesion, and integrin signalling. It has been demonstrated that the level of Talin-1 in the serum of colon cancer patients was significantly higher than that of healthy controls. Talin-1 may be a valuable biomarker for colon cancer, which may be essential for the early detection, especially in combination with other markers in population screenings that are currently used to detect the colon cancer.
Human Cripto-1 (CR-1) is an embryonic gene, belonging to the EGF-CFC gene family, which is necessary for promoting early stages of embryonic development. CR-1 is a good example of a multifaceted embryonic protein that is re-expressed in most human tumors, particularly colorectal tumor, but not detected in normal adult human tissues. García-Sanmartín et al. showed that Cripto-1 expression was significantly correlated with worse prognosis in CRC, and was an independent prognostic factor.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Sherouk Ahmed Sayed, Assistant lecturer
- Phone Number: +201009922949 +201123232632
- Email: shrookabozaid@gmail.com
Study Locations
-
-
Asyut Governorate
-
Asyut, Asyut Governorate, Egypt, 17777
- Assuit University Hospital
-
Contact:
- Sherouk Ahmed
- Phone Number: 01123232632
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group(1)
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum Talin-1 measurement in colorectal cancer patients
Time Frame: From enrollment up to one week
|
measuring serum level of talin-1 in colorectal cancer patient to compare its level with healthy control
|
From enrollment up to one week
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Serum Cripto-1 measurement in colorectal cancer patients
Time Frame: From enrollment up to one week
|
From enrollment up to one week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SHROOK
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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