ArtiSential® for Rectal Cancer Surgery
- Disease/Condition
- Rectal Cancer
- Drug/Device/Intervention
- ArtiSential®
- Study type
- Observational
- Intervention type
- device
- Primary sponsor
- Seoul National University Hospital
- Location
- Seoul, South Korea
- Phase
- N/A
- Start date
- May 01, 2012
- End date
- Mar 31, 2023
- Enrollment
- 93 participants
Operation time
This study aimed to assess efficacy of ArtiSential® in reducing laparoscopic rectal cancer
 surgery duration. We retrospectively reviewed the data of patients who underwent laparoscopic
 low or ultralow anterior resection for primary mid-to-low rectal cancer, performed by a
 single surgeon in 2012-2022. Patients were divided into groups, use group vs. non-use group,
 based on the use or non-use of the ArtiSential®. The total mesorectal excision quality and
 resection margin status did not differ between the groups. ArtiSential® reduced operative
 time without impairing surgical quality or oncologic outcomes.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06236282
- Type
- Device Trial
Access comprehensive clinical trial information for NCT06236282 through Pure Global AI's free database. This phase not specified trial is sponsored by Seoul National University Hospital and is currently Completed. The study focuses on Rectal Cancer. Target enrollment is 93 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.