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Screening Effect of Dual-energy CT Combined With Nasopharyngeal Endoscopy for Screening Nasopharyngeal Carcinoma

Z

Zhongshan City People's Hospital

Status

Enrolling

Conditions

Nasopharyngeal Carcinoma

Treatments

Procedure: participants will undergo dual-energy CT and endoscopy

Study type

Observational

Funder types

Other

Identifiers

NCT05884983
NPC-PRO-004

Details and patient eligibility

About

All participants will be tested for EBV-related biomarkers, including EBNA1-IgA, VCA-IgA, and BNLF2b total antibody (P85-Ab), and participants with high serologic risk will be selected based on serologic test results, and dual-energy CT will be performed first for high-risk screening subjects, and dual-energy CT will be performed first for the high-risk group to record dual-energy CT examinations of those suspected of nasopharyngeal carcinoma, and then endoscopy was performed on the high-risk group to record those suspected of nasopharyngeal carcinoma under endoscopy, and finally biopsies were taken for positive lesion sites indicated by dual-energy CT and suspicious lesion sites found by endoscopy to clarify the diagnosis.

Enrollment

12,000 estimated patients

Sex

All

Ages

30 to 69 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subject residents in Zhongshan City
  • Subject has no medical record of nasopharyngeal carcinoma
  • Subject is able to comprehend, sign, and date the written informed consent document to participate in the study
  • Subject has psychical condition and well consciousness, and also accept and cooperate with the follow-up of this study

Exclusion criteria

  • Subject has heavy cardiovascular, liver or kidney disease
  • Subject has contraindications to nasopharyngeal endoscopy
  • Subject has contrast media allergy

Trial design

12,000 participants in 1 patient group

Screening cohort
Description:
30-69 years old healthy participants in Zhongshan
Treatment:
Procedure: participants will undergo dual-energy CT and endoscopy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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