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Genital Neoplasms, Male clinical trials

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NCT ID: NCT03210376 Completed - Clinical trials for Malignant Neoplasms of Female Genital Organs

Neuromuscular Blockade on Shoulder Pain of Elderly

Start date: November 17, 2017
Phase: Phase 4
Study type: Interventional

Insufflation pressure (IP) is the creation of a pressure barrier of air/gas within the abdomen to allow the surgeon more space to work during abdominal surgery. Shoulder pain is a common complaint from patients who have had abdominal surgery and the pain is thought to be related to the use of IP. In addition to anesthesia (which keeps you asleep during surgery), the current standard practice is to block the nerve-muscle junction with a type of drug called neuromuscular blockade (NMB) which paralyzes the abdominal muscles. This means that a lower level of insufflation pressure is needed by the surgeon. To reverse the effects of NMB after surgery, a drug called neostigmine is given. The goal of this clinical research study is to compare the use of standard-of-care moderate NMB and neostigmine to the use of deep NMB and a drug called Sugammadex when given to elderly patients (patients who are 65 years of age or older) who are scheduled to have robotic abdominal surgery. "Deep" and "moderate" in this study refers to the dose or strength of the NMB given. This is an investigational study. Sugammadex and neostigmine are FDA approved and commercially available for the reversal of NMB. It is considered investigational to compare Sugammadex and neostigmine to learn if the use of one or the other in elderly patients can reduce the level of shoulder pain after surgery. Up to 100 participants will be enrolled in this study. All will take part at MD Anderson.

NCT ID: NCT02740127 Completed - Clinical trials for Malignant Neoplasms of Male Genital Organs

Evaluate Use of Caudal Nerve Blocks in Adult Penile Prosthesis

Start date: June 2016
Phase: Phase 3
Study type: Interventional

During penile prosthesis surgery, patients are given general anesthesia in combination with other pain drugs. A caudal nerve block (CNB) is a local anesthetic injected near the tailbone, in addition to general anesthesia, which can lower the need for pain drugs. The goal of this clinical research study is to learn how effective CNBs are in patients who are having penile prosthesis surgery compared to patients who only have general anesthesia by studying how long you stay in the hospital and the level of pain you have after surgery. This is an investigational study. The general anesthesia and CNB used in this study are FDA approved and commercially available. It is considered investigational to compare the effectiveness of CNBs in penile prosthesis surgery to general anesthesia alone. The study doctor can explain how the study drugs are designed to work. Up to 104 participants will be enrolled in this study. All will take part at MD Anderson.

NCT ID: NCT02192333 Completed - Depression Clinical Trials

Survivorship Care in Reducing Symptoms in Young Adult Cancer Survivors

Start date: August 3, 2015
Phase: N/A
Study type: Interventional

This randomized clinical trial studies survivorship care in reducing symptoms in young adult cancer survivors. Survivorship care programs that identify the needs of young adult cancer survivors and ways to support them through the years after treatment may help reduce symptoms, such as pain, fatigue, sleep disturbance, depression, and distress, in young adult cancer survivors.

NCT ID: NCT01316458 Completed - Prostatic Neoplasm Clinical Trials

Glivec in Prostate Cancer Patients With Rising PSA Following Radical Prostectomy

Start date: June 2003
Phase: Phase 2
Study type: Interventional

To investigate the ability of 600 mg of Glivec®, given once daily by mouth to patients with rising PSA following radical prostatectomy, to produce a sustained biochemical response during the first 6 months of treatment.

NCT ID: NCT00210041 Completed - Clinical trials for Genital Neoplasms, Male

Phase 2 Study of Association Gemcitabine-Cisplatin to Treat Penis Epidermoid Carcinoma

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether association Gemcitabine-Cisplatin is effective in the treatment of penis epidermoid carcinoma loco-regionally advanced or metastatic.