Prevalence of Neglected Side Effects to Radical Prostatectomy

NCT ID: NCT01742962

Last Updated: 2014-07-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

396 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-12-31

Study Completion Date

2013-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this exploratory data collection is to strengthen our knowledge of some of the rarer distresses following surgical removal of the prostate. In general these are:

* Side effects related to sexuality, including:
* Altered perception of orgasm,
* Orgasm associated pain,
* Penile shortening and deformity.
* Side effects related to urinary incontinence.
* Urinary tract infection after operation.
* Influence of distress on sexual quality of life.
* Influence of distress on the patient´s sex drive.

In addition information on a range of demographics and information on the patient´s erectile function will be collected.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Approximately 1 out of 6 men will, at some point of their life become diagnosed with prostate cancer. Treatment options included medication therapy, radiation therapy, and surgery. This data collection aims to gather information on some of the lesser known distresses experienced by patients following surgical removal of the prostate gland.

Erectile dysfunction and urinary incontinence remain common, but thoroughly investigated side effects. Thus they will not be of primary interest here, but considered factors for correlation. During the last couple of years, a series of lesser known side effects have come to investigators attention. These include altered perception of orgasm, orgasm related pain, sexual-related urinary incontinence, and shortening -and impairing deviations of the penis. Few studies have investigated these side effects, and clear knowledge of why, and how often these problems arise, remain scarce. This study will contribute to that knowledge.

In addition, the questionnaire will include a series of exploratory questions, concerning lower urinary tract infections, treatment satisfaction, alcohol and urinary incontinence, reasons for abandoning treatment for erectile dysfunction, and an assessment of libido prior to and after radical prostatectomy.

The data collection will include approximately 400 patients from the department of urology at the University Hospital in Herlev, Copenhagen, Denmark. A questionnaire will be sent to patients together with a stamped addressed envelope in order to optimize the response rate. Results will be kept in a separate database from personal information.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Prostate Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Radical prostatectomy for prostate cancer

Prior treatment with open or robot assisted laparoscopic prostatectomy.

Radical prostatectomy for prostate cancer

Intervention Type PROCEDURE

Prior treatment with open or robot assisted laparoscopic prostatectomy.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Radical prostatectomy for prostate cancer

Prior treatment with open or robot assisted laparoscopic prostatectomy.

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* All patient who have undergone radical prostatectomy at the department of urology, Copenhagen University Hospital, Herlev, between 3 months and 3 years before initiation of the study.

Exclusion Criteria

* Incontinence associated with sexual activity Prior to surgery
* Peyronies disease Prior to surgery
* Orgasm related pain Prior to surgery
* Anorgasmia Prior to surgery
Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Copenhagen University Hospital at Herlev

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Anders U. K. Frey, Stud.Med.

Role: PRINCIPAL_INVESTIGATOR

Copenhagen University Hospital in Herlev, Denmark

Mikkel M. Fode, Dr.

Role: STUDY_DIRECTOR

Copenhagen University Hospital in Herlev, Denmark

Jens Sønksen, Professor

Role: STUDY_CHAIR

Copenhagen University Hospital in Herlev, Denmark

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Copenhagen University Hospital in Herlev, Denmark

Herlev, Herlev, Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

H-2-2012-FSP43

Identifier Type: OTHER

Identifier Source: secondary_id

2007-58-0015 / HEH.750.19-31

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Prehabilitation for Prostate Cancer Surgery
NCT02036684 COMPLETED PHASE1/PHASE2