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The Relationship Between Bone Pelvis Measurements and Erectile Function in Patients Who Had Nerve-Sparing Robot-Assisted Radical Prostatectomy Operation

NCT ID: NCT06179316

Last Updated: 2023-12-21

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

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-12-15

Study Completion Date

2024-07-01

Brief Summary

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In order to evaluate the relationship between bone pelvis measurements and erectile function in patients who underwent nerve-sparing robot-assisted radical prostatectomy, bone pelvis measurements will be measured from MRI images of the patients before the operation and their erection quality will be evaluated with the IIEF-5 form. The erection quality of the same patients will be evaluated with the IIEF-5 form in the 3rd and 6th months after the operation. And it will be evaluated whether there is a relationship between the erection quality of the patients before and after the operation and their bone pelvis measurements.

Detailed Description

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Conditions

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Erectile Dysfunction

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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preoperative patients

Robot Assisted Radical Prostatectomy

Intervention Type PROCEDURE

Performing radical prostatectomy operation using robotic equipment while preserving bilateral nerve bundles

Patients in the 3rd postoperative month

No interventions assigned to this group

Patients in the 6th month postoperatively

No interventions assigned to this group

Interventions

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Robot Assisted Radical Prostatectomy

Performing radical prostatectomy operation using robotic equipment while preserving bilateral nerve bundles

Intervention Type PROCEDURE

Other Intervention Names

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Bilateral Nerve-Sparing Robot-Assisted Radical Prostatectomy Operation

Eligibility Criteria

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Inclusion Criteria

* Having bilateral nerve-sparing robot-assisted radical prostatectomy operation
* Having a regular sexual life

Exclusion Criteria

* Having received neoadjuvant therapy
* Having a history of radiotherapy to the pelvic area
* The need to receive postoperative hormono-radiotherapy
Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Ankara Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Ali Kaan Yildiz

principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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AŞH.AKYILDIZ.007

Identifier Type: -

Identifier Source: org_study_id