Clinical Trials Logo

Clinical Trial Summary

Postoperative gastrointestinal complications following ESD, EMR, and EFTR procedures, such as gastrointestinal bleeding, diverticula, fistulas, perforations, and stent fixation, can be effectively treated through gradual endoscopic procedures. The technical limitations of traditional endoscopic hemoclips restrict their application. Although endoscopic suturing techniques are emerging, most are still in the exploratory phase. Therefore, the investigators have developed metal-reinforced teeth for hemoclips. This initial clinical study aims to validate the safety, feasibility, and effectiveness of reinforced teeth in clinical applications. The investigators also aim to explore the uses and limitations of this technology. The primary outcomes are the technical success rate and the clinical success rate.


Clinical Trial Description

With the advancement of endoscopic technology, gastrointestinal defects following endoscopic submucosal dissection (ESD), mucosal resection (EMR), and full-thickness resection (EFTR), as well as complications such as gastrointestinal bleeding, diverticula, fistulas, perforations, and even fixation of esophageal stents, can gradually be treated through endoscopic procedures. This approach avoids surgical incisions and reduces patient recovery time. Traditional endoscopic hemoclips have limited application due to constraints such as arm extension distance, size of the clip's front teeth, and closing force. Therefore, the investigators have developed metal-reinforced teeth for hemoclips. This initial clinical study aims to validate the safety, feasibility, and effectiveness of reinforced teeth in clinical applications. The investigators also aim to explore the uses and limitations of this technology. The primary outcome measures include technical success rate and clinical success rate. Additionally, the investigators closely monitor procedure time, the number of clip uses during the procedure, and postoperative adverse events during follow-ups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06285955
Study type Observational
Source Beijing 302 Hospital
Contact Yan Liu, MD
Phone +8613911798288
Email 13911798288@163.com
Status Recruiting
Phase
Start date January 15, 2024
Completion date August 31, 2024

See also
  Status Clinical Trial Phase
Completed NCT01175161 - Postpartum Intrauterine Device Study N/A
Recruiting NCT04047524 - A Trimodal Prehabilitation Study for Patients Undergoing Major Abdominal Surgery N/A
Completed NCT04310995 - Different Anti-Spastic Therapy Strategies After CABG Using Radial Artery Grafts Phase 4
Not yet recruiting NCT05957289 - Multidimensional Rehabilitation Intervention in Colorectal Cancer Survivors - a Pilot Study N/A
Enrolling by invitation NCT02993432 - High Volume Foleys Increasing Vaginal Birth Pilot Trial N/A
Completed NCT01437033 - Breath Test for Chemicals (Volatile Organic Compounds)
Completed NCT05480423 - Online Mindfulness-based Intervention on Parents of Children With Attention Deficit/Hyperactivity Disorder N/A