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Hydrocele clinical trials

View clinical trials related to Hydrocele.

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NCT ID: NCT04870242 Completed - Appendicitis Clinical Trials

Studding the Implementation of ERAS Protocols in Pediatric Surgery

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

this is a retrospective cohort, descriptive study, investigating the role of ERAS protocols, in pediatric surgery and evaluate the feasibility and effectiveness of implementing these protocols

NCT ID: NCT04406077 Completed - Hydrocele Clinical Trials

The Use of Ligasure (r) for Hydrocelectomy Surgery

Start date: February 18, 2018
Phase: N/A
Study type: Interventional

Hydrocele is a condition of fluid retention around the testes, which causes swallowing, pain, with interfering with the normal testes function. however, during activity, this can interfere with everyday activity (running, sexual intercourse). The treatment for hydrocele I surgical. The study aim to test the safety and efficacy of the Ligasure (r) device for cutting and coagulating tissues during hydrocelectomy.

NCT ID: NCT03677453 Completed - Hypospadias Clinical Trials

Interactive Perioperative Teaching Platform (IPTP)

Start date: October 10, 2018
Phase: N/A
Study type: Interventional

The proposed study will assess whether an interactive perioperative teaching platform (IPTP) provided to families of patients undergoing ambulatory pediatric surgery will reduce families' anxiety, and improve satisfaction and understanding, relative to current practice. The IPTP will educate patient families on the continuum of their child's surgical experience, from arriving at the hospital through registration, the operating room (OR), and the hospital floor. An active video format will be used to provide instructions for navigating the hospital; describe induction of anesthesia and the surgical procedure; and provide post-surgery and post-discharge instructions for pain management. A comparison cohort of patients undergoing surgery without access to the IPTP will be recruited to assess the benefits of the IPTP for improving metrics of family satisfaction, preoperative anxiety, and postoperative understanding of discharge instructions.

NCT ID: NCT03575377 Completed - Hernia Clinical Trials

Opioid Use, Storage, and Disposal Among Pediatric Patients After Surgery

Start date: June 7, 2018
Phase: N/A
Study type: Interventional

Opioids are an important component of post-operative pain management among children, but are often prescribed in excess and rarely disposed of appropriately. The lack of prompt and proper opioid disposal after recovery from surgery is contributing to the opioid crisis in Ohio by placing children at risk of accidental ingestion of opioids remaining in the home and allowing for unused opioids to be diverted for non-medical use. The investigators propose to reduce the burden of the opioid crisis in Ohio by testing a strategy to increase proper opioid disposal by families of children undergoing outpatient surgery. The investigators will test the impact of a novel opioid disposal mechanism, the Deterra® drug deactivation system, after pediatric surgical operations. This system deactivates pills, liquids, or patches, allowing for their disposal in the home garbage. The investigators propose to evaluate the effectiveness of providing Deterra® bags to families of children having surgery on their disposal of excess opioids. The investigators will perform a randomized controlled trial (RCT) to test the effectiveness of Deterra® to improve opioid disposal among families of children having outpatient surgery at Nationwide Children's Hospital.

NCT ID: NCT02040389 Completed - Anxiety Clinical Trials

Visual Guidelines and Tutoring in Pediatric Urological Surgery

Start date: March 2014
Phase: N/A
Study type: Interventional

The aim of this study is checking impact of visual guidelines (picture book) and tutoring in pediatric urologic surgery

NCT ID: NCT01896076 Completed - Inguinal Hernia Clinical Trials

The Caudal Space in Children: Ultrasound Evaluation

Start date: June 2013
Phase: N/A
Study type: Observational

Caudal anesthesia is commonly employed in pediatrics to produce postoperative analgesia in low abdominal or urologic surgery. An exact understanding of the anatomy of the sacral area including sacral hiatus and surrounding structures is crucial to the success of caudal block. The aim of this study is to evaluate the anatomy of the caudal space in pediatrics by ultrasound evaluation.

NCT ID: NCT01872364 Completed - Hernia Clinical Trials

Dominican Republic Mission Cost Analysis

Start date: May 2013
Phase: N/A
Study type: Observational

Expenditures on material supplies and medications constitute the greatest per capita costs for surgical missions. We hypothesized that supply acquisition at nonprofit organization cost would lead to significant cost-savings compared to supply acquisition at US academic institution costs from the provider perspective for hernia repairs and minor procedures during a surgical mission in the Dominican Republic.

NCT ID: NCT01698268 Completed - Inguinal Hernia Clinical Trials

Study of Transverse Abdominis Plane (TAP) Block in Children Undergoing Hydrocelectomy and/or Hernia Repair Surgery

TAP
Start date: February 2012
Phase: Phase 2
Study type: Interventional

Study measures the difference in pain after hernia &/or hydrocele repair based on site of local anesthesia injection.

NCT ID: NCT00130091 Completed - Hernia, Inguinal Clinical Trials

The Addition of Clonidine to 0.2% Ropivacaine for Wound Instillation After Minor Lower Abdominal Surgery in Children

Start date: September 2009
Phase: Phase 2
Study type: Interventional

The current study will compare the effects on postoperative pain relief of "freezing" (ropivacaine 0.2 %) alone and in combination with clonidine for a nerve block in children undergoing hernia repair. The researchers anticipate that the addition of clonidine to "freezing" will result in prolongation of postoperative pain relief in children undergoing hernia repair compared to "freezing" used alone.