Vascular Changes Of Patients Undergoing Laparoscopic Radical Prostatectomy

Prostatic Neoplasms Clinical Trial

Official title:

Valuation Of Vascular Changes And Their Impact On Erectile Function By Penile Doppler Ultrasound And Analysis Of The Quality Of Life Of Patients Undergoing Laparoscopic Radical Prostatectomy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03241758
• Other study ID #: RadicalDoppler
• Status: Completed
• Phase: N/A
• First received: August 3, 2017
• Last updated: August 4, 2017
• Start date: November 29, 2011
• Est. completion date: August 2, 2017

Study information

• Verified date: August 2017
• Source: Corporacion Parc Tauli
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A study designed to evaluate vascular changes after radical laparoscopic prostatectomy using Doppler ultrasound and the impact of such changes on erectile function and quality of life of patients. The baseline study will be compared with the study one year after surgery.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 110
• Est. completion date: August 2, 2017
• Est. primary completion date: August 2, 2017
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Male patients with prostate cancer who underwent laparoscopic radical prostatectomy

Exclusion Criteria:

• Patients who were not interested in their sexual function and refused to perform this study

• Patients who required adjuvant or salvage treatment for their prostate cancer (radiation therapy, chemotherapy or androgen deprivation therapy) during follow-up.

Related Conditions & MeSH terms

• Erectile Dysfunction
• Erectile Dysfunction Following Radical Prostatectomy
• Prostatic Neoplasms

Intervention

Diagnostic Test:
• Doppler ultrasound
Basal Doppler ultrasound and Doppler ultrasound one year after radical prostatectomy

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Corporacion Parc Tauli

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Left and right Cavernous artery diameter	mm	1 year
Primary	Left and right Systolic velocity cavernous artery	cm/s	1 year
Primary	Left and right Diastolyc velocity cavernous artery	cm/s	1 year