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Salivary Biomarkers for the Early Diagnosis of Esophageal Cancer

Salivary Biomarkers for the Early Diagnosis of Esophageal Cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110336
Enrollment
Unknown
Registered
2025-10-13
Start date
2025-10-13
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Esophagus cancer

Interventions

Gold Standard:Results from the endoscopic examination and histopathological testing
Index test:A panel of esophageal cancer-specific biomarkers comprising salivary miRNAs and oral microorganisms.

Sponsors

Changhai Hospital, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Subjects must meet all of the following criteria:(1) Aged >= 18 years; (2) Have undergone or are scheduled to undergo esophageal endoscopy, with available results from the endoscopic examination or histopathological testing; (3)Willing to participate in the study and capable of providing written informed consent.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they meet any of the following criteria: (1) Women who are currently lactating or pregnant; (2) History of esophageal cancer; (3) Previous receipt of any therapeutic intervention for esophageal cancer (e.g., surgery, radiotherapy, chemotherapy, targeted therapy, or immunotherapy); (4) Diagnosis of any other primary malignancy within the past 5 years (except for individuals with a history of other cancers who have completed treatment and remained disease-free for over 5 years, who may be enrolled); (5) Severe impairment of cardiac, pulmonary, hepatic, or renal function, or any other severe systemic disease; (6) Active infectious diseases such as Hepatitis B, Hepatitis C, or HIV infection; (7) Presence of psychiatric or psychological disorders that would compromise the ability to comply with study requirements; (8) Inability to meet the sample collection requirements for the study's detection assays; (9) Any other condition deemed by the investigator to make the participant unsuitable for the clinical study.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;Accuracy;

Countries

China

Contacts

Public ContactWang Luowei

Changhai Hospital

wangluoweimd@126.com+86 139 0183 3088

Outcome results

None listed

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