Condition: Colorectal Anastomosis · Sponsor: Fundación para la Investigación del Hospital Clínico de Valencia
Patients whom meet all eligibility criteria will be assigned random 1:1 to one of the following arms: * ECPS group: Echelon Circular™ Powered Stapler (n=270) * MCS Group: manual circular staplers (n=270) Patients will be followed during 30 days in order to evaluate the primary endpoint.
This description comes directly from the study's public registry record.
Vicente Pla Martí · +34 669204303 · vplamarti@yahoo.es
Always discuss trial participation with your own doctor first.
| Consorci Corporació Sanitària Parc Taulí de Sabadell | Sabadell, Barcelona, Spain | Not Yet Recruiting |
| Hospital General Universitario Gregorio Marañón | Madrid, Spain | Recruiting |
| Hospital Clínico Universitario Virgen de la Arrixaca | Murcia, Spain | Recruiting |
| Hospital Clínico Universitario de Valencia | Valencia, Spain | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06578065