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Prostatectomy clinical trials

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NCT ID: NCT06119568 Completed - Nephrectomy Clinical Trials

Safety and Performance Assessment of a First Four Arms on Demand Open Robotic Solution for Assisted PN, RN and RP

Start date: November 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this clinical investigation is to evaluate the safety and performance of the Bitrack System and its corresponding ElectroSurgical Endoscopic (ESE) instruments and Non-ElectroSurgical Endoscopic (NESE) instruments and accessories in patients with the indication of a robot assisted laparoscopic Radical Nephrectomy (RN), Partial Nephrectomy (PN) or Radical Prostatectomy (RP), as applicable. HYROS-PRnP is a confirmatory study in which the hypothesis of the primary endpoint is that the ESE/NESE instruments perform as intended when controlled by Bitrack System which operates exclusively under surgeon's orders. The study shall refer to safety and performance of Bitrack System together with its accessories and corresponding ESE/NESE instruments. This study includes the data collected up to 30 days post-surgery and provides the evidence that the tested medical devices fulfill the GSPR.

NCT ID: NCT06020287 Completed - Prostate Neoplasm Clinical Trials

The Robot-Assisted Laparoscopic Radical Prostatectomy Combined Anterior and Posterior Approach

Start date: September 1, 2020
Phase:
Study type: Observational

The goal of this observational study was to compare the perioperative outcomes, postoperative urinary control rates and positive surgical margin (PSM) rates of the robot-assisted laparoscopic radical prostatectomy combined anterior and posterior approach (AP-RARP) with the Retzius-sparing approach (RS-RARP) and anterior approach (anterior-RARP) in the treatment of prostate cancer. The main question it aims to answer was: • The early therapeutic efficacy of the robot-assisted laparoscopic radical prostatectomy combined anterior and posterior approach Participants has been underwent: - AP-RARP - RS-RARP - anterior-RARP Researchers compared the three groups to see if AP-RARP combines the advantages of anterior and posterior RARP and is a feasible surgical option for the treatment of prostate cancer.

NCT ID: NCT05700487 Completed - Clinical trials for URINARY INCONTINENCE

EFFECT ON QUALITY OF LIFE AFTER PROSTATECTOMY

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Aim: This study was conducted to determine the effect of pelvic floor exercises (PTE) on urinary incontinence and quality of life (QOL) after radical prostatectomy (RP). Methods: This randomized controlled, single-blind, experimental study was completed with a total of 33 RP patients, 18 of whom were interventions, and 15 were controls. The intervention group was given pelvic floor exercises (PTE) training in the preoperative period, regular PTE was performed three times a day for six months in the postoperative period, and the continuity of the exercises was checked by telephone. On the other hand, no intervention was applied to the control group other than routine treatment.

NCT ID: NCT05242198 Completed - Prostatectomy Clinical Trials

Rectus Sheath Block May Relieve Urethral Catheter Pain

Start date: March 15, 2022
Phase: N/A
Study type: Interventional

This study aimed to investigate the analgesic efficacy of rectus sheath block and its effect on urethral catheter discomfort in robotic prostatectomy operations.

NCT ID: NCT03884335 Completed - Prostatectomy Clinical Trials

Radical Laparoscopic Prostatectomy. Enhanced Recovery After Surgery (ERAS) Program

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

Current trends are based on the implementation of enhanced recovery programs (ERP) for most surgical procedures. The transversus abdominis plane (TAP) block has been demonstrated as an effective analgesic alternative in abdominal surgeries. The goal of this study was to compare analgesic efficacy of the TAP block against epidural technique in patients who underwent laparoscopic radical prostatectomy (LRP) surgery in an ERP setting. This study was performed between October 2016 and May 2018

NCT ID: NCT03721029 Completed - Clinical trials for Urinary Incontinence

Intraoperative Nerve Monitoring During Robotic-assisted Radical Prostatectomy

Start date: November 21, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether the use of intraoperative nerve monitoring during robotic-assisted radical prostatectomy (RARP) can predict and improve post-surgery urinary continence and erectile function.

NCT ID: NCT03714984 Completed - Clinical trials for Pelvic Floor Disorders

The Efficacy of Pre-operative Educational Pelvic Floor Intervention on Urinary Continence

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

Prostate cancer is the most common type of cancer between male population and urinary incontinence (UI) is the most common of long-term sequelae. Nowadays, robotic prostatectomy became the surgery standard but there is still discrepant results regards the incidence of UI and there is a lack of studies about the use of pelvic floor rehabilitation in this population. Our study aims to assesses the efficacy of preoperative educational method in urinary incontinence after robotic prostatectomy.

NCT ID: NCT03624465 Completed - Prostatectomy Clinical Trials

Prospective Clinical Study of the Levita Magnetics Surgical System Used for Prostatectomy Surgery

Start date: August 13, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the Levita Magnetic Surgical System in patients undergoing prostatectomy surgery.

NCT ID: NCT03618693 Completed - Pain Clinical Trials

Impact of Perioperative Analgesia in Prostatectomy Patients on Early Quality of Recovery (SPITALIDO)

SPITALIDO
Start date: August 13, 2018
Phase: N/A
Study type: Interventional

The rationale behind this RCT is to assess within 24 hours after surgery the quality of recovery of prostatectomy patients treated with 3 different analgesia concepts (intraoperative spinal analgesia, transversus abdominis plane block, intravenous lidocaine administration) using the quality of recovery (QoR) 15 questionnaire.

NCT ID: NCT03607279 Completed - Prostatectomy Clinical Trials

Comparison of Plasma Neutrophil Gelatinase - Associated Lipocalin (NGAL) Levels

Start date: January 2017
Phase:
Study type: Observational [Patient Registry]

The purpose of the study is to compare the effect of two surgical techniques (open vs robotic assisted) on plasma levels of NGAL (neutrophil gelatinase-associated lipocalin) after radical prostatectomy.