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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05980403
Other study ID # WDRY2023-K115
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 18, 2023
Est. completion date September 18, 2024

Study information

Verified date January 2024
Source Renmin Hospital of Wuhan University
Contact Yongshun Chen, MD
Phone +8615327122084
Email yongshun2007@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Accurate assessment of lymph node status in superficial esophageal squamous cell carcinoma is of great significance for preventing undertreatment and overtreatment. However, the accuracy of the commonly used preoperative imaging methods for evaluating lymph node status is not high, and it is urgent to develop a prediction model that can predict the risk of individual lymph node metastasis to assist in clinical decision-making. In this context, investigators intend to retrospectively collect the clinical and pathological data of 300 patients with superficial esophageal squamous cell carcinoma, construct a lymph node metastasis risk prediction model. In addition, investigators are also preparing to prospectively collect tissue samples from 30 patients with superficial esophageal squamous cell carcinoma to further explore the mechanism of lymph node metastasis.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date September 18, 2024
Est. primary completion date June 18, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Patients diagnosed with esophageal cancer in Renmin Hospital of Wuhan University from 2013 to 2022. 2. Histopathological diagnosis was squamous cell carcinoma. 3. T1NxM0. 4. Received endoscopic resection or esophagectomy. Exclusion Criteria: 1. Patients who received neoadjuvant therapy. 2. Positive surgical margin. 3. Prior malignancy requiring active treatment within the previous 3 years except for locally curable cancers that have been apparently cured. 4. Lack of complete histopathological information.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
China Renmin hosptial of Wuhan University Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Yongshun Chen

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lymphatic metastases The primary end point was the presence of lymph node metastases in surgically resected specimens (= 15 resected lymph nodes), or the development of metastases during follow-up including local recurrence and distant metastasis (AJCC 8th). In cases of an endoscopic resection prior to surgical resection, the tumor was found in the endoscopic resection specimen and lymph node status in the surgical resection specimen. When no additional surgery was performed after endoscopic resection, the development of metastases during follow-up was used as a surrogate end point. Through study completion, an average of 2 year
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