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NCT05404685Completed

Partial Nephrectomy in Low Pressure

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

Source: ClinicalTrials.gov · Last updated 13 Jun 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
280 (actual)
First submitted
27 Apr 2022
Start date
4 Oct 2022
Primary completion date
29 Apr 2024
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT05404685

What you commit to

  • Study type: Interventional
  • Participants enrolled: 280
  • From 4 Oct 2022 to the primary completion date, 29 Apr 2024
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Daily chronic pain-killers intake for another indication than the kidney tumor and intended to be maintained at the time of surgery

Other

  • Person deprived of liberty
  • Person under trusteeship, curatorship or legal guardianship
  • Refusal of consent or participation in the UroCCR project and the P-NeLoP ancillary trial
  • \-

Who the study is looking for

  • Male or Female aged of 18 and over
  • Planned transperitoneal RAPN for tumor with AirSeal system.
  • Affiliation to or beneficiary of the French social security
  • Patient in capacity and willing to accurately report pain-killer intakes in the first postoperative 7 days.
  • Free, informed and written consent signed by the patient and the investigating physician (at the latest on the day of inclusion and before any examination required by the research).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU d Angers
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AngersFranceUnknown status
Centre hospitalier Universitaire de Bordeaux
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BordeauxFranceUnknown status
CHU de CAEN
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CaenFranceUnknown status
Hopital Henri Mondor
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CréteilFranceUnknown status
Hopital Claude Huriez
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LilleFranceUnknown status
Institut Paoli-Calmettes
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MarseilleFranceUnknown status
CHU de Nice
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NiceFranceUnknown status
Hopital Pitie-Salpetriere
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ParisFranceUnknown status
Hôpital bicêtre
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ParisFranceUnknown status
Polyclinique Francheville Périgueux
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PérigueuxFranceUnknown status
CHU de Poitiers
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PoitiersFranceUnknown status
Clinique La Croix Du Sud
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Quint-FonsegrivesFranceUnknown status
CHU de Rennes
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RennesFranceUnknown status
CHRU de Strasbourg
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StrasbourgFranceUnknown status
CHU de Tours
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ToursFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.