Trials / Withdrawn
WithdrawnNCT04811833
Gastrointestinal Anastomosis Using MonoPlus® Suture
Assessment of MonoPlus® Suture Material for Anastomosis in the Gastrointestinal Tract. A Prospective, Multi-centric, International, Single-arm, Observational Study in Daily Practice
- Status
- Withdrawn
- Phase
- —
- Study type
- Observational
- Enrollment
- 0 (actual)
- Sponsor
- Aesculap AG · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary aim of this study is to collect clinical data on the performance of MonoPlus® suture applied in routine clinical practice. Diverse parameters are to be used to assess the safety and efficacy of MonoPlus® suture for gastrointestinal anastomosis construction. This study has been designed to implement an action within the framework of a proactive Post Market Clinical Follow up (PMCF) activity.
Conditions
- Gastrointestinal Stromal Tumors
- Gastrointestinal Neoplasms
- Digestive System Neoplasm
- Stomach Tumor
- Small Intestine Tumor
- Colon Tumor
- Rectum Tumor
Timeline
- Start date
- 2022-07-01
- Primary completion
- 2023-12-01
- Completion
- 2023-12-01
- First posted
- 2021-03-23
- Last updated
- 2023-04-05
Locations
2 sites across 1 country: Spain
Source: ClinicalTrials.gov record NCT04811833. Inclusion in this directory is not an endorsement.