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Radical Prostatectomy clinical trials

View clinical trials related to Radical Prostatectomy.

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NCT ID: NCT05332340 Completed - Prostate Cancer Clinical Trials

Safety, Tolerability and Pharmacokinetics (PK) Evaluation of BZ371A, Topically Administered

Start date: November 16, 2022
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate pharmacokinetics, safety and tolerability profile of BZ371A topically administered in healthy patients.

NCT ID: NCT04862533 Completed - Prostate Cancer Clinical Trials

Effect of Beta-alanine and Pelvic Floor Muscle Training on Urinary Incontinence After Radical Prostatectomy (BELA)

BELA
Start date: February 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of beta-alanine in combination with pelvic floor muscle training (PFMT) compared to PFMT plus placebo in men undergoing radical prostatectomy.

NCT ID: NCT04587505 Completed - Quality of Life Clinical Trials

Effect of Epidural Anesthesia and Analgesia on Quality of Recovery After Radical Prostatectomy.

QoR
Start date: April 1, 2019
Phase: Phase 4
Study type: Interventional

Postoperative quality of recovery (QoR) could be related to anesthesia and postoperative analgesia. This study is exploring early QoR after radical prostatectomy in the two groups of anesthesia. The first group had a light general anesthesia with lumbal epidural anesthesia and postoperative epidural analgesia with morphine and ropivacaine. The second group had general anesthesia and a continuous postoperative analgesia with tramadol. The postoperative QoR was evaluated 24 hours after surgery.

NCT ID: NCT03639389 Completed - Postoperative Pain Clinical Trials

Postoperative Pain, Recovery and Discharge Following Robot-assisted Laparoscopic Prostatectomy

RAPID
Start date: January 1, 2019
Phase: Phase 3
Study type: Interventional

Prostate cancer is the commonest cancer form in men in Northern Europe. Management of the cancer often includes surgical removal of the primary tumor. In the last 5-10 years, robot assisted laparoscopic prostatectomy (RALP) has become common. Good pain relief is central to early mobilization and greater patient satisfaction. Randomized controlled studies on pain relief following RALP are few and the role of spinal analgesia in pain management following robotic surgery has not been described. Techniques available for pain relief following RALP include spinal anesthesia with or without opiates, intravenous analgesia with morphine or a multimodal pain management technique using a combination of several analgesics. Spinal anesthesia and analgesia reduces the surgical stress and inflammatory response following laparoscopic colorectal surgery and may offer similar benefit even during RALP. Early perioperative complications may cause postoperative morbidity following robotic surgery, and sometimes delay home discharge. Since all robotic operations in the pelvic region are performed in a deep Trendelenberg position, this can even have negative consequences for the heart, brain and the lungs. Cardiac complications in the form of minimal cardiac injury or mild heart failure have not been previously studied following RALP. Additionally, patients are sometimes delirious in the early postoperative period following RALP. The precise cause for this remains unclear and may be related to pain, cognitive dysfunction or an urge to pass urine despite a urinary catheter. In addition to good postoperative pain relief, early postoperative mobilization and home discharge are important milestones in recovery of full function following major surgery. With improvement in surgical technique, the time has come to evaluate if RALP can be performed on an ambulatory basis. The main aims of this study are: 1. Can RALP be performed on an ambulatory basis and patients ready to be discharged home at 8 pm? 2. To determine if spinal anesthesia reduces pre-discharge pain intensity, stress response and other perioperative side effects. 3. Is sufentanil or fentanyl the analgesic of choice when administered spinally together with bupivacaine as an analgesic. 4. To determine the frequency and severity of cardiac and respiratory complications in the steep Trendelenberg position during RALP. 5. To assess the quality of recovery, quality of life and activities of daily living following ambulatory RALP?

NCT ID: NCT03587402 Completed - Clinical trials for Urinary Incontinence

Effects of Transcutaneous Perineal Stimulation Versus Anal Stimulation

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

This study evaluates whether surface perineal stimulation is as effective as anal stimulation in reducing urinary incontinence secondary to radical prostatectomy. Half of participants will receive a treatment with surface perineal stimulation, while the other half will receive a treatment with anal stimulation.

NCT ID: NCT00953277 Completed - Prostate Cancer Clinical Trials

Study of Nerve Reconstruction Using AVANCE in Subjects Who Undergo Robotic Assisted Prostatectomy for Treatment of Prostate Cancer

Start date: August 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if it is technically feasable to repair nerves that are injured as part of a planned surgical removal of the prostate and the surrounding tissue in subjects with prostate cancer. The study will also examine the long term outcomes on erectile function, continence and overall quality of life in the enrolled subjects.