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Hernia, Inguinal clinical trials

View clinical trials related to Hernia, Inguinal.

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NCT ID: NCT04623580 Recruiting - Inguinal Hernia Clinical Trials

Flemish Inguinal and Femoral Hernia Prospective Registry

FLIPR
Start date: January 1, 2018
Phase:
Study type: Observational [Patient Registry]

Prospective registry. The purpose of this clinical trial will be to measure surgical outcome parameters (e.g. recurrence, chronic pain and other quality indicators) after inguinal hernia repair using Patient Reported Outcome Measures (PROMs) in the short- and long-term.

NCT ID: NCT04591470 Completed - Clinical trials for Male Infertility Due to Antisperm Antibody

Influence of Inguinal Hernia Repair on Sperm Autoimmunity

SPERMAR
Start date: June 1, 2020
Phase:
Study type: Observational

Influence of inguinal hernia repair on sperm autoimmunity using MAR test

NCT ID: NCT04551924 Recruiting - Clinical trials for Inguinal Hernia Repair

A Trial of HR18034 in Inguinal Hernia Repair

Start date: October 1, 2020
Phase: Phase 1
Study type: Interventional

Phase I, randomized, double-blind, comparator-controlled study to assess the safety, PK, and efficacy of single postsurgical application of HR18034 compared with Naropin®

NCT ID: NCT04541316 Completed - Inguinal Hernia Clinical Trials

Neo-angiogenesis in Inguinal Henia Implant ProFlor

Start date: January 2013
Phase:
Study type: Observational

The investigation is aimed at specifically demonstrating the ingrowth of newly formed vascular elements within ProFlor, a 3D dynamic responsive implant for inguinal hernia repair

NCT ID: NCT04532983 Completed - Inguinal Hernia Clinical Trials

Short Term Outcome of Laparoscopic Trans-abdominal Preperitoneal Inguinal Hernia Repair Without Mesh Fixation

professor
Start date: July 1, 2018
Phase: N/A
Study type: Interventional

comparison between two groups of participants suffering inguinal hernia each group 23 individual all underwent laparoscopic trans-abdominal inguinal hernia repair first group received mesh fixation the second underwent no fixation , results of follow up in the first year were compared together

NCT ID: NCT04504461 Completed - Inguinal Hernia Clinical Trials

Ambulatory Laparoscopic Inguinal Hernioplasty: Feasibility and Cost Analysis

Start date: August 1, 2015
Phase:
Study type: Observational

Laparoscopic inguinal hernia repair has become one of the elective techniques, attributing the advantages of minimally invasive procedures to it. However, the high costs related to the need for hospitalization and materials make them a limitation at the time of its indication. The objective is to evaluate the feasibility of performing this procedure in an outpatient surgery center and the cost analysis of an outpatient procedure regarding the same in the setting of hospitalization.

NCT ID: NCT04494087 Recruiting - Inguinal Hernia Clinical Trials

The Effect of Preoperative Explanatory Videos in Total Extraperitoneal Inguinal Hernioplasty on Information Providing: a Multicenter Randomized Controlled Trial

Start date: May 18, 2022
Phase: N/A
Study type: Interventional

The use of electronic media in informed consent giving has become increasingly important in recent years. Due to the easy access to information via electronical media, patients are primed in a heterogeneous manner concerning expectations and wishes regarding surgical interventions. Inherent to its nature elective interventions are critically questioned as there is time for information gathering and reflection. In this study, the investigators set out to investigate the effect of an educational video as a supporting element in the process of informed consent giving for one the most frequently performed interventions in general surgery, namely inguinal hernia repair. In a multi-center setup, eligible patients for primary inguinal hernia repair will be randomly assigned to 1 of 3 groups. The intervention video provides basic principles of endoscopic extraperitoneal hernia repair. The second video is similar in length and design and displays general aspects of day surgery in the two study centres. The third group's link will lead to the digital version of the informed consent. Primary outcomes will consist of 1) score in a multiple choice test assessing gain of knowledge regarding hernia repair, 2) difference in the State-Trait Anxiety Inventory (STAI) and 3) patient satisfaction questionnaire (ICF, Picker Institute, Germany) as assessed 1-2 days after the first consultation.

NCT ID: NCT04491526 Recruiting - Inguinal Hernia Clinical Trials

Study to Prevent Postoperative Urinary Retention

STOP-POUR
Start date: November 1, 2020
Phase: Phase 4
Study type: Interventional

Post-operative urinary retention (POUR) is a common complication after inguinal hernia repair with a reported incidence up 34%. It can be described as the inability to initiate urination or properly empty one's bladder following surgery. It is usually self-limited, but it requires the use of catheterization to empty the bladder in order to prevent further injury to the bladder or kidneys and to relief the discomfort of a full bladder. Tamsulosin is a medication that is commonly used in men with urinary symptoms related to an enlarged prostate. There is some evidence to suggest that it may also potentially be beneficial for preventing post-operative urinary retention. The purpose of this study is to determine if tamsulosin ("TAMSULOSIN Mepha Ret Depocaps 0.4 mg") is effective in preventing post-operative urinary retention following endoscopic total extraperitoneal inguinal hernia repair and its impact on hospital length of stay.

NCT ID: NCT04437784 Completed - Clinical trials for Bilateral Inguinal Hernia

Laparoscopic Versus Open Mesh Repair of Bilateral Primary Inguinal Hernia

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

The best approach for simultaneous repair of bilateral inguinal hernia is controversial. The aim of this study is to compare the outcomes after laparoscopic versus open mesh repair of bilateral primary inguinal hernia

NCT ID: NCT04434378 Terminated - Clinical trials for Post Operative Urinary Retention

Tamsulosin to Prevent Postoperative Urinary Retention in Laparoscopic Inguinal Hernia Repair

Start date: November 16, 2017
Phase: Phase 4
Study type: Interventional

To investigate the effect of tamsulosin on the development of post-operative urinary retention (PUR) after elective laparoscopic inguinal hernia repair (LIHR). This will be accomplished by administering a pre-operative dose of tamsulosin. The primary outcome is the rate of urinary retention necessitating straight catheterization or insertion of foley catheter prior to discharge.