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Laparoscopic Liver Resection

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified October 2007 by IRCCS San Raffaele.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00553033
First Posted: November 2, 2007
Last Update Posted: November 2, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
IRCCS San Raffaele
  Purpose
The aim of this study is to evaluate the feasibility and safety of laparoscopic liver surgery.

Condition Intervention
Tumors Procedure: Laparoscopic liver surgery

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Prospective Evaluation of Laparoscopic Liver Resection

Further study details as provided by IRCCS San Raffaele:

Primary Outcome Measures:
  • Perioperative Morbidity and mortality [ Time Frame: Perioperative ]

Secondary Outcome Measures:
  • Patient satisfation [ Time Frame: Perioperative ]
  • Patients satisfaction [ Time Frame: Postoperative ]

Estimated Enrollment: 40
Study Start Date: September 2005
Estimated Study Completion Date: December 2008
Groups/Cohorts Assigned Interventions
A Procedure: Laparoscopic liver surgery
Ultrasonic dissector, harmonic scalpel

Detailed Description:
Perioperative course of patients undergoing liver resection is evaluated.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients udergoing liver resection for benign or malignant tumors
Criteria

Inclusion Criteria:

  • benign or malignant tumors
  • tumor size less than 12 cm

Exclusion Criteria:

  • Operations that required laparotomic procedures
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00553033


Contacts
Contact: Luca Aldrighetti, M.D, PhD 390226437806 aldrighetti.luca@hsr.it

Locations
Italy
Department of Surgery - Liver Unit, Scientific Institute San Raffaele Recruiting
Milan, Italy, 20132
Contact: Luca Aldrighetti, M.D PhD    +39-02-2643-7808    aldrighetti.luca@hsr.it   
Sponsors and Collaborators
IRCCS San Raffaele
Investigators
Study Director: Luca Aldrighetti, M.D PhD Department of Surgery - Liver Unit, Scientific Institute San Raffaele
  More Information

Publications:
ClinicalTrials.gov Identifier: NCT00553033     History of Changes
Other Study ID Numbers: LPSLIVER1
First Submitted: November 1, 2007
First Posted: November 2, 2007
Last Update Posted: November 2, 2007
Last Verified: October 2007

Keywords provided by IRCCS San Raffaele:
Patients must be candidable to liver resection

Additional relevant MeSH terms:
Liver Extracts
Hematinics