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Robotic Laparoscopic Radical Prostatectomy

Robotic Laparoscopic Radical Prostatectomy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00292019
Enrollment
20
Registered
2006-02-15
Start date
2004-03-04
Completion date
2016-06-30
Last updated
2017-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Brief summary

This is a pilot study to evaluate the role of RALRP in the management of localized prostate cancer.

Detailed description

To establish a robotic-assisted laparoscopic radical prostatectomy programme at the University of Western Ontario/London Health Sciences Centre and to critically evaluate the role of this programme in the management of localized prostate cancer in surgical candidates Details of surgical procedure, operative outcome, patient outcome including quality of life will be collected.

Interventions

PROCEDURELaparoscopic

Patients with prostate cancer who are eligible for a radical prostatectomy will have their surgery conducted with the aid of surgical robots.

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Informed Consent 2. Locally confined, stage T1a, T2a or T2b prostate cancer 3. Aged 40-65 and judged by the study doctor to be a suitable candidate for a radical prostatectomy. 4. Serum prostate specific antigen equal to or less than 10mg/ml 5. Histologically confirmed adenocarcinoma of the prostate 6. Gleason score equal to or less than 7 7. Life expectancy of greater than 10 years. 8. Prostate size on TRUS measurement less than 40 grams

Exclusion criteria

1. Patients who have undergone prior hormone therapy. 2. Patients with a previous transurethral resectioning of the prostate (TURP) 3. History of other cancers other than basal cell carcinoma. 4. Patients with any prior abdominal surgery. 5. Any condition, or history of illness or surgery than, in the opinion of the investigator, might confound the results of the study or pose additional risk to the patient (eg significant cardiovascular conditions) 6. Patients with a large median lobe of the prostate. -

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026