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Study on the value of image enhanced endoscopic technology in early screening of esophageal squamous cell carcinoma in patients with oral squamous cell carcinoma

Study on the value of image enhanced endoscopic technology in early screening of esophageal squamous cell carcinoma in patients with oral squamous cell carcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091889
Enrollment
Unknown
Registered
2024-11-05
Start date
2024-05-21
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Repeated esophageal cancer in patients with oral squamous cell carcinoma

Interventions

Gold Standard:Pathology
Index test:Image enhanced endoscopic technology

Sponsors

Shanghai Ninth Peoples’ Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Newly diagnosed oral squamous cell carcinoma patients who have been clinically diagnosed have pathological evidence and clinical staging meets the indications for radical surgical treatment; (2) Between the ages of 18 and 85; (3) Sign an informed consent form, cooperate with follow-up and review, and have good compliance.

Exclusion criteria

Exclusion criteria: (1) Other oral tumors confirmed by pathology as non squamous cell carcinoma; (2) Previous history of oral squamous cell carcinoma surgery and radiation therapy; (3) Previous history of digestive tract tumors such as esophagus and stomach; (4) Individuals with contraindications for gastrointestinal endoscopy examination; (5) Individuals with severe primary diseases such as cardiovascular, cerebrovascular, pulmonary, hepatic, renal, and hematopoietic systems (6) Individuals with abnormal mental states (such as anxiety, depression, schizophrenia, etc.); Individuals who are unable to fully obtain informed consent due to intellectual or behavioral impairments; (7) Pregnant or lactating women; (8) Individuals with a history of iodine allergy or hyperthyroidism are not suitable for iodine staining examination; (9) Frequent changes in work environment or place of residence or other situations that may lead to loss of access; Patients participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
sensitivity;Specificity;positive predictive value ;

Countries

China

Contacts

Public ContactLei Wang

Shanghai Ninth Peoples’ Hospital, Shanghai Jiao Tong University School of Medicine

wanglei197886@sina.com+86 21 2327 1699

Outcome results

None listed

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