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NCT07088744Not yet recruiting

Comparison of the Sensitivity of pCLE and Pathological Biopsy Before ESD

Comparison of the Sensitivity of Probe-based Confocal Laser Endomicroscopy and Pathological Biopsy Before Endoscopic Submucosal Dissection

Source: ClinicalTrials.gov · Last updated 28 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Pathological biopsy before endoscopic submucosal dissection (ESD) the gastric lesion plays an important role in differentiating the pathological nature of the lesion and guiding treatment decisions. However, due to the influence of the materials used, the sensitivity of pathological biopsy is not satisfactory. Confocal Laser Endomicroscopy (CLE) is a technology that integrates a confocal microscope into an endoscope. It enables the acquisition of high-resolution microscopic images of the mucosal layer in real-time (with a magnification of up to 1000 times), and it is an optical biopsy technique. It has unique value in the determination of the pathological nature of gastric lesions. The main purpose of this study is to compare the sensitivity of pathological biopsy and CLE in differentiating the pathological nature of gastric lesions.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
169 (estimated)
First submitted
19 Jul 2025
Start date
30 Jul 2025
Primary completion date
31 Aug 2025
Lead sponsor
Changhai Hospital
NCT number
NCT07088744

What you commit to

  • Study type: Observational
  • Planned participants: 169
  • From 30 Jul 2025 to the primary completion date, 31 Aug 2025
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe cardiac or pulmonary dysfunction, impaired renal function, coagulopathy, pregnancy or lactation, allergy to fluorescein, and inability to provide informed consent.

Who the study is looking for

  • patients aged 18 to 85 years who were scheduled for endoscopic submucosal dissection due to early-stage gastric cancer were consecutively enrolled.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
West China Hospital of Sichuan University
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ChengduChinaUnknown status
Guangxi Zhuang Autonomous Region People's Hospital
Coordinator of this site? Confirm its status
NanningChinaUnknown status
The First Affiliated Hospital of Naval Medical University
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
Northern Theater Command Hospital
Coordinator of this site? Confirm its status
ShenyangChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.