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Spots Global Cancer Trial Database for Partial Nephrectomy in Low Pressure

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Trial Identification

Brief Title: Partial Nephrectomy in Low Pressure

Official Title: Randomised Study to Assess the Feasibility and Outcomes of Robotic Assisted Partial Nephrectomy in Low Pressure With AirSeal

Study ID: NCT05404685

Study Description

Brief Summary: The main objective is to prospectively assess the impact of low insufflation pressure using AirSeal system (7mm Hg) during RAPN on post-operative patient pain (main location and intensity), 24 hours after surgery. The study will be conducted among 15 centers of the French research network on kidney cancer UroCCR.

Detailed Description: Minimally invasive route for PN is recommended to offer patients ERAS and day-case pathways leading to the best possible recovery. In this setting, pain management is crucial and every innovation supposed to offer a benefit has to be assessed. For transperitoneal laparoscopic procedures, the level and stability of the insufflation pressure will influence the quality of the pneumoperitoneum and may impact the feasibility of the surgery as well as intra and post-operative outcomes. It is universally recognized that the lower insufflation pressure, the better. However, a balance has usually to be found between technical feasibility of the surgery and lowest acceptable insufflation pressure. The AirSeal system aims to generate a stable pneumoperitoneum even in case of active gaz succion by the surgeon's assistant. The investigators then hypothesize that RAPN would be feasible and safe even in low pressure (7mm Hg) and may decrease post-operative patients' pain. The investigators plan to describe the feasibility of Low Pressure RAPN at 7mm Hg (LP-RAPN) and assess its intra and post-operative outcomes including pain and recovery on a patient perspective. This will be achieved comparatively to RAPN performed at standard insufflation pressure of 12 mm Hg and through a single blinded randomized trial design. The project has been developed and will be conducted within the framework of the French research network on kidney cancer UroCCR (www.uroccr.fr). INCa has been supporting this multidisciplinary network since 2011 and the web-based shared clinical and biological national database on kidney cancer UroCCR will be used.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

CHU d'Angers, Angers, , France

Centre Hospitalier Universitaire de Bordeaux, Bordeaux, , France

CHU de Caen, Caen, , France

Hopital Henri-Mondor, Créteil, , France

Hôpital Claude Huriez, Lille, , France

Institut Paoli-Calmettes, Marseille, , France

CHU de Nice, Nice, , France

Hôpital Pitié-Salpétrière, Paris, , France

Hôpital bicêtre, Paris, , France

CHU de Poitiers, Poitiers, , France

Polyclinique Francheville Périgueux, Périgueux, , France

Clinique La Croix du Sud, Quint-Fonsegrives, , France

CHU de Rennes, Rennes, , France

CHRU de Strasbourg, Strasbourg, , France

CHU de Tours, Tours, , France

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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