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NCT05301699 Clinical Trial

Development and Validation of a Web-based Nomorgam to Predict Postoperative Complications

Gastric Cancer Clinical Trial

Official title:
Development and Validation of a Web-based Nomorgam to Predict Postoperative Complications After Radical Gastrectomy Among Elderly Gastric Cancer Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05301699
Other study ID # XMiao
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2021
Est. completion date March 30, 2022

Study information
Verified date May 2022
Source Nanjing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The incidence of complications after gastrectomy remains high among elderly patients with gastric cancer. The investigators sought to establish and validate a web-based nomorgam for predicting total complications among elderly patients undergoing resection of gastric cancer.

Recruitment information / eligibility
Status Completed
Enrollment 582
Est. completion date March 30, 2022
Est. primary completion date March 30, 2022
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - diagnosed with gastric cancer by endoscopy or pathology - planned to receive radical surgery for the first time - aged 60 or older Exclusion Criteria: - received preoperative radiotherapy or chemotherapy - with other sites of malignant tumors

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• data analysis; validating the nomogram
Not Applicable. Our study did not involve intervention

Locations
Country Name City State
China Nanjing medical university Nanjing

Sponsors (1)
Lead Sponsor Collaborator
Nanjing Medical University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative complications during hospitalization the investigators captured it from electronic medical records about 3 weeks
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