NCT00695773

Brief Summary

This study is aimed at discovering the differences in outcomes, regarding quality of life issues(continence, impotence) of patients who have had either laparoscopic or open surgical technique for prostate cancer.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
158

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2006

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2006

Completed
2.4 years until next milestone

First Submitted

Initial submission to the registry

June 10, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 12, 2008

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2008

Completed
Last Updated

December 1, 2008

Status Verified

November 1, 2008

Enrollment Period

2.8 years

First QC Date

June 10, 2008

Last Update Submit

November 28, 2008

Conditions

Keywords

Prostate Cancer SurgeryLaparoscopic surgery for Prostate CancerProstatectomyUrologic Surgical Procedures

Outcome Measures

Primary Outcomes (1)

  • The post-surgical questionnaire information collected will be used to determine any benefits to future patients who are to undergo a prostatectomy

    Post Surgical

Eligibility Criteria

Sexmale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

A Lahey Clinic IRB approved database and current clinic population of patients having a laparascopic or open prostatectomy

You may qualify if:

  • Subjects who have undergone a prostatectomy

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Lahey Clinic, Inc.

Burlington, Massachusetts, 01805, United States

Location

Study Officials

  • John A. Libertino, M.D.

    Lahey Clinic, Inc.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Sponsor Type
OTHER

Study Record Dates

First Submitted

June 10, 2008

First Posted

June 12, 2008

Study Start

February 1, 2006

Primary Completion

November 1, 2008

Study Completion

November 1, 2008

Last Updated

December 1, 2008

Record last verified: 2008-11

Locations