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Spots Global Cancer Trial Database for Prediction of Abdominal Complications After GastroEnterological Surgery

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Trial Identification

Brief Title: Prediction of Abdominal Complications After GastroEnterological Surgery

Official Title: Abdominal Infectious Complications After Gastrointestinal Surgery in China: a Multi-centered Prospective Registry

Study ID: NCT03828266

Interventions

No intervention

Study Description

Brief Summary: The aim of this multi-centered study is to understand the epidemiology of infectious complications after gastrointestinal surgery in China. In total, 17 centers from China will prospectively register their patients undergo gastric or colorectal surgeries. Patient demographic data, operation information, and postoperative data including the infectious complications and the outcomes will be registered. We expect to include 2000 gastric and 2000 colorectal patients within one year and the study is expected to be finished in 2020.

Detailed Description: All participating hospital will log in on a website based e-CRF system. Researchers need to register the patient information that three time-points: admission, after surgery, after discharge. The detailed registered information includes: I. Basic and surgical information: Age, height, weight, history of abdominal surgery, ASA score, surgical procedure, extent of lymph node dissection, extent of resection, time of surgery, amount of bleeding, whether it is emergency surgery, whether it is combined with organ resection, whether it is palliative resection, whether combined with preoperative treatment, whether combined with preoperative infection and intraoperative complications. II. Postoperative information: Primary lesion histological type, margin, pathological stage (pTNM); other complications, postoperative death and discharge time, CRP, PCT, WBC levels. III. Abdominal Infection information: Abdominal infection (Y/N), anastomotic leakage (Y/N), intervention, outcome.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Peking University Cancer Hospital, Beijing, Beijing, China

Fujian Medical University Union Hospital, Fuzhou, Fujian, China

Xiamen University First Hospital, Xiamen, Fujian, China

Guangdong People's Hospital, Guangzhou, Guangdong, China

The First Affilliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China

South Hospital, Guanzhou, Guangdong, China

Nanchang University First Hospital, Nanchang, Jiangxi, China

Jilin University Second Hospital, Changchun, Jilin, China

Dalian Medical University First Hospital, Dalian, Liaoning, China

Qinghai University Affiliated Hospital, Xining, Qinghai, China

Shandong Provincial Hospital, Jinan, Shandong, China

Qingdao University Affiliated Hospital, Qingdao, Shandong, China

Fudan University Cancer Hospital, Shanghai, Shanghai, China

Huashan Hospital, Shanghai, Shanghai, China

Ruijin Hospital, Shanghai, Shanghai, China

Zhongshan Hospital, Shanghai, Shanghai, China

Xi'an Jiao Tong University First Hospital, Xi'an, Shanxi, China

Hangzhou First Hospital, Hangzhou, Zhejiang, China

Run Run Shaw Hospital, Hangzhou, Zhejiang, China

Contact Details

Name: Ziyu Li, MD PhD

Affiliation: Peking University Cancer Hospital & Institute

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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