Role of Programmed Death Ligand 1 in Colorectal Cancer
SPDL1
the Role of Programmed Death Ligand 1 in Diagnosis of Colorectal Cancer
1 other identifier
observational
90
0 countries
N/A
Brief Summary
- 1.\- Evaluation of diagnostic importance of soluble programmed death ligand-1 in patient with recently diagnosed as Colorectal cancer at different stages of disease .
- 2.Correlation of SPDL-1 level and clinco-pathological data of patients at presentation .
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2025
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 19, 2025
CompletedFirst Posted
Study publicly available on registry
July 28, 2025
CompletedStudy Start
First participant enrolled
August 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
July 28, 2025
July 1, 2025
1.1 years
July 19, 2025
July 19, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Study the expression level of sPDL 1 in colorectal cancer by ELISA
Correlate the expression level of sPDL-1 and stage of disease
baseline
Interventions
enzyme- linked immunesorbent assay ( ELISA ) was used to measure soluble programmed death ligand-1 level
Eligibility Criteria
Cases and controls will be recruited from clinical pathology department at South Egypt Cancer Institute, and Assuit University Hospital
You may qualify if:
- \. Patients did not undergo colorectal surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Shao W, Xu Y, Lin S, Gao J, Gao J, Wang H. The potential of soluble programmed death-ligand 1 (sPD-L1) as a diagnosis marker for colorectal cancer. Front Oncol. 2022 Aug 16;12:988567. doi: 10.3389/fonc.2022.988567. eCollection 2022.
PMID: 36052227BACKGROUND
Biospecimen
serum or plasma
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- resident doctor
Study Record Dates
First Submitted
July 19, 2025
First Posted
July 28, 2025
Study Start
August 1, 2025
Primary Completion (Estimated)
August 30, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
July 28, 2025
Record last verified: 2025-07