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Hernia, Femoral clinical trials

View clinical trials related to Hernia, Femoral.

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NCT ID: NCT05920200 Recruiting - Chronic Pain Clinical Trials

Factors Influencing the Results of Treatment in Patients With Hernias of Various Localizations

Start date: January 9, 2020
Phase:
Study type: Observational

The study attempts to quantify the relative risks for acute postoperative pain, complications rate, chronic postoperative pain (CPIP) and recurrence rate after different methods of repair of groin, umbilical and incisional hernia depending on surgical technique, mesh type and fixation suture material. For this purpose the investigators will analyze data from the Kalinigrad Hernia Registry (KHR).

NCT ID: NCT05306496 Recruiting - Inguinal Hernia Clinical Trials

Laparoscopic Inguinal and Femoral heRniA rePaIr Using Pre-shapeD 4DMESH® (4DLap)

Start date: August 4, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and performance of the 4DMESH® used in (robot-assisted) laparoscopic inguinal and femoral hernia repair. The goal of the study will be achieved by assessing the prevalence of recurrences, pain, quality-of-life (QoL), return to daily activities and work and groin symptoms, and by reporting of peri- and postoperative complications in a prospectively maintained database.

NCT ID: NCT04839848 Completed - Chronic Pain Clinical Trials

Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty

Start date: September 1, 2012
Phase:
Study type: Observational [Patient Registry]

The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) after Lichtenstein repair of groin hernia, depending on mesh type and fixation suture material. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

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: NCT04228536 Completed - Hernia, Inguinal Clinical Trials

Chronic Pain After Groin Hernia Surgery in Women

Start date: September 1, 2012
Phase:
Study type: Observational [Patient Registry]

The goal of this study was to evaluate chronic pain and reoperation rates due to recurrence after groin hernia surgery in women compared to men and surgical method.

NCT ID: NCT04009213 Completed - Inguinal Hernia Clinical Trials

A Clinical Study to Evaluate the Clinical Performance and Safety of LiquiBand FIX8® Versus AbsorbaTackā„¢ for Hernia Mesh Fixation and Peritoneal Closure in Groin Hernia Repair

Start date: August 22, 2019
Phase: N/A
Study type: Interventional

This is a multi-center, randomized controlled trial of 284 subjects (142 in each group). Patients will be blinded to the fixation method used. The objective of this study is to compare the efficacy and safety of the LiquiBand FIX8® device to the tack-based control device (AbsorbaTackā„¢) for laparoscopic groin hernia (inguinal or femoral) repair. The primary outcome measure is an improvement in pain score measured by VAS at 6 months. Secondary outcomes include the ability to affix hernia mesh, the ability to approximate the peritoneum, recurrence rate, and quality of life (Carolina Comfort Scale).

NCT ID: NCT03755219 Completed - Recurrence Clinical Trials

Mesh and Mesh Fixation in Laparoscopic Groin Hernia Surgery

Start date: January 1, 2005
Phase:
Study type: Observational [Patient Registry]

The study attempts to quantify the relative risks for recurrence depending on complex combinations of plausible risk factors, in particular mesh, mesh fixation, hernia size and hernia type. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

NCT ID: NCT02920307 Completed - Recurrence Clinical Trials

Study of Laparoscopic Inguinal Hernia Repair

Start date: May 2010
Phase: N/A
Study type: Interventional

Although mesh fixation has been associated to an increased incidence of nerve injury and involves increased operative costs, many surgeons feel that fixation is necessary to reduce the risk of hernia recurrence. The aim of this study is to evaluate the outcomes of laparoscopic herniorrhaphies performed with and without mesh fixation at our institution.

NCT ID: NCT02751190 Completed - Hernia, Inguinal Clinical Trials

Chronic Pain After Groin Hernia Repair

Start date: September 1, 2013
Phase: N/A
Study type: Observational [Patient Registry]

In the present study the investigators aimed to investigate the relationship between surgical methods and chronic pain in over 20 000 patients who underwent groin hernia repair in Sweden

NCT ID: NCT01170780 Completed - Inguinal Hernia Clinical Trials

Dexamethasone Versus Placebo in Optimizing the Postoperative Period After Laparoscopic Inguinal Hernia Repair

Start date: August 2010
Phase: Phase 3
Study type: Interventional

Does corticosteroid (dexamethasone) have an effect on the postoperative period after laparoscopic hernia repair, when it comes to pain, postoperative nausea and vomiting and convalescence. This randomized, double-blinded study compares dexamethasone versus placebo. The patients are recommended one day of convalescence. The medicine or placebo is given before operation. The patients fill out questionnaire before operation and three hours after operation and in the following three days. The patients also register when they return to normal activities and work.