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Registry and Database Lap Prostatectomy

This study has been suspended.
Study NCT00169676.   Last updated on September 16, 2008.   Information provided by Indiana Kidney Stone Institute

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Descriptive Information Fields
Brief Title  Registry and Database Lap Prostatectomy
Official Title  Laparoscopic Radical Prostatectomy: A Registry and Database
Brief Summary

Recently, many centers have begun offering laparoscopic radical prostatectomy (LRP) as a minimally invasive therapy for localized prostate cancer.1-6 LRP may offer the advantages of improved neurovascular bundle sparing, a more precise urethrovesical anastomosis, shorter hospitalization, and decreased convalescence.

Our group at Methodist Urology, LLC has extensive experience in laparoscopy and in treating prostate cancer and are planning to offer LRP. We intend to maintain a registry and database to document the outcomes with LRP.

Detailed Description

Prostate cancer is the second leading cause of cancer death in men today. An estimated 220,900 new cases will be diagnosed in 2003 according to the American Cancer Society.7 Prostate cancer will account for one-third of the new cancer diagnoses in men in 2003. Prostate specific antigen (PSA), a sensitive screening method for prostate cancer, has helped diagnose prostate cancer at earlier stages. Stamey et al. found that the diagnosis of prostate cancer in patients with T1c disease (no abnormalities on digital rectal examination but elevated PSA) increased from10% in 1988 to 73% in 1996 and the increase in organ confined cancers increased from 40% to 75% over the same time period.8

Current surgical options for organ confined prostate cancer include open radical retropubic prostatectomy, open radical perineal prostatectomy, radioactive seed implantation, and radiation therapy. Open radical retropubic prostatectomy was pioneered in 1947 by Millin but what was slow to gain widespread acceptance secondary to associated morbidity.9-13 Refinement of the retropubic approach by Walsh has greatly improved outcomes, making it the most common surgical approach for radical prostatectomy.14, 15

As with other procedures, interest in the laparoscopic approach for radical prostatectomy developed in hopes of minimizing patient morbidity. In 1992, Schuessler et al performed the first LRP but the technical difficulties of the procedure at that time prohibited the widespread application of this technique.16 In 1998, Guillonneau et al introduced the Mountsouris technique in which a transperitoneal approach was used to perform the LRP.17, 18 Other groups have used this approach and even adapted this technique to perform extraperitoneal approaches to LRP.1, 2, 4, 5, 19, 20 Many centers are currently offering LRP as primary therapy for organ confined prostate cancer.

All curative surgical therapies for prostate cancer, whether performed in an open or laparoscopic manner, can result in impotence and/or incontinence. Incontinence can be treated with simple measures, such as muscle strengthening exercises, or if more bothersome, can be treated with surgical therapy. Impotence can be treated with medications or, if needed, surgery.

The relative risk of having positive surgical margins in patients undergoing open radical retropubic prostatectomy compared to laparoscopic radical prostatectomy is not known. Preliminary publications regarding laparoscopic radical prostatectomy report rates of positive surgical margins (13-25%) that are similar to open radical prostatectomy (11-46%).2, 5, 6, 19, 21-28 However, long-term follow-up is not available for patients undergoing laparoscopic radical prostatectomy, so the impact of positive margins on long-term survival is not known.

Study Phase
Study Type  Observational
Study Design  Cohort, Prospective
Primary Outcome Measure  To create a registry and database for the treatment of localized prostate cancer with LRP. To record long term outcomes for patients undergoing Laparoscopic Radical Prostatectomy. [ Time Frame: One year ] [ Designated as safety issue: No ]
Secondary Outcome Measure 
Condition  Prostate Cancer
Intervention  Other: observation
MEDLINE PMIDs
Links click here to view other studies being done by Methodist Urology This link exits the ClinicalTrials.gov site
Recruitment Information Fields
Recruitment Status  Suspended
Enrollment  100
Start Date  June 2003
Completion Date April 2009
Eligibility Criteria 

Inclusion criteria:

  • Patient of Methodist Urology in Indianapolis, IN
  • Ability to give informed consent
  • Biopsy proven diagnosis of prostate cancer without local extension or metastatic disease (Clinical T2 or less in the TNM classification)

Exclusion criteria:

  • Major abdominal surgery precluding a safe laparoscopic approach
  • Bleeding diathesis or anticoagulation
  • Medical disease (such as cardiovascular or pulmonary diseases) precluding general anesthesia/laparoscopy
  • Transplanted kidney in the pelvis
  • Radiation therapy to pelvis
  • Morbid obesity
Gender Male
Ages 18 Years and older
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00169676
Organization ID 03-040
Secondary IDs ††
Study Sponsor  Indiana Kidney Stone Institute
Collaborators ††
Investigators 
Principal Investigator:     Larry Munch, MD     Methodist Urology, LLC    
Information Provided By Indiana Kidney Stone Institute
Verification Date September 2008
First Received Date  September 9, 2005
Last Updated Date September 16, 2008

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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