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Hernia, Inguinal clinical trials

View clinical trials related to Hernia, Inguinal.

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NCT ID: NCT03820570 Completed - Inguinal Hernia Clinical Trials

Comparison Open Lichtenstein Repair and Totally Extraperitoneal Herniorrhaphy

Start date: January 1, 2012
Phase: N/A
Study type: Interventional

comparison of early and long term results of open lichtenstein repair and totally extraperitoneal herniorrhaphy for primary inguinal hernias.

NCT ID: NCT03765268 Completed - Inguinal Hernia Clinical Trials

Neurectomy Vs Nerve Sparing in Open Inguinal Hernia Repair

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

It is a randomized controlled trial in which we are treating inguinal hernia patients with mesh hernioplasty and either neurectomy of iliohypogastric nerve and ilioinguinal neurectomy or preservation comparing post operative acute or chronic pain

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: NCT03739060 Completed - Quality of Life Clinical Trials

Impact of TENS on Postoperative Pain and Quality of Life After Inguinal Hernia Repair

TENS1
Start date: August 1, 2018
Phase: N/A
Study type: Interventional

Lichtenstein herniorrhaphy still remains one of the most often performed inguinal hernia repair techniques. It is frequently associated with acute postoperative and chronic pain. Due to insufficient effect of non-steroidal anti-inflammatory drugs, they are often overdosed. However opioids have many side effects. Interventional treatment, such as transversus abdominis plain (TAP) block requires an additional intervention and has relatively short effect, also could not be applied in outpatient conditions. The hypoalgesic effect of transcutaneous electric nerve stimulation (TENS) is well known for many years, but effectiveness during postoperative period is still controversial and maybe therefore didn't come to daily practice. However it could be a promising part of multi-modal pain treatment for hernia patients. This study analyse the hypoalgesic effect of TENS and its impact on hernia specific quality of life (QoL) after Lichtenstein hernia repair. Aim#1 To determine whether use of TENS is effective for acute postoperative pain relief. Aim#2 To determine whether use of TENS have impact on hernia specific QoL in early and late postoperative period. Aim#3 To identify factors associated with effectiveness/ineffectiveness of TENS procedures. Aim#4 To determine whether a psychological condition (depression, anxiety and pain catastrophisation) is somehow associated with TENS effectiveness.

NCT ID: NCT03734224 Completed - Quality of Life Clinical Trials

Inguinal Hernia Operation and Postoperative Pain

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

Inguinal hernia is a common disease, which is treated surgically when symptomatic. Pain after open inguinal hernia surgery can affect the patient significantly and weaken their quality of life. The aim of this study is to find out if the choice of mesh affects postoperative pain and therefore causes more contacts to the health care center. Our goal is also to find out how the pain affects the patients´ quality of life.

NCT ID: NCT03713047 Completed - Chronic Pain Clinical Trials

A National Center for Persistent Severe Pain After Groin Hernia Repair

Q5Y
Start date: January 1, 2010
Phase:
Study type: Observational

This prospective, consecutive cohort study presents nationwide 5-year outcome data on patients with severe persistent pain after groin hernia repair (SPG). The inclusion criteria were SPG-related impairment of physical and social life. Two-hundred-four out of 222 patients (92%) were analyzed. Relevant surgical records were obtained, and examinations were by standardized clinical and neurophysiological tests. Patients demonstrating pain sensitivity to pressure algometry in the groin were evaluated regarding exploratory surgery, while patients with putative neuropathic pain received pharmacotherapy. Questionnaires at baseline (Q0) and five-year (Q5Y) were used in outcome-analyses of pain-intensity (numeric rating scale [NRS] 0-10) and the pain-related effect on the activity-of-daily-living (Activities Assessment Scale, AAS).

NCT ID: NCT03678272 Completed - Inguinal Hernia Clinical Trials

Comparative Study of Inguinodynia After Inguinal Hernia Repair

Start date: April 2013
Phase: N/A
Study type: Interventional

To evaluate the postoperative pain and the relapse after the repair of the inguinal hernia by Lichtenstein technique with four different mesh types with different types of fixation in patients undergoing major ambulatory surgery.

NCT ID: NCT03665883 Completed - Hernia, Inguinal Clinical Trials

Use of Diathermy Versus Blunt Dissection in TEP for Inguinal Hernia

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

There is a long debate whether monopoloar or blunt dissection should be adopted in TEP to minimise the chance of seroma formation. This study aims at study the effect on seroma formation (and pre-peritoneal drain output) by 2 techniques in randomised controlled trial.

NCT ID: NCT03640598 Completed - Inguinal Hernia Clinical Trials

Erector Spinae Versus Ilioinguinal/ Ilio-hypogastric Block in Children Undergoing Inguinal Surgeries

Start date: August 20, 2018
Phase: N/A
Study type: Interventional

Investigators aim to compare the efficacy of US-guided II/IH nerve block versus US-guided ES block for pediatric unilateral inguinal hernia repair with respect to postoperative analgesia

NCT ID: NCT03623893 Completed - Inguinal Hernia Clinical Trials

Hernia Exploration oR Not In Infants Analysis

HERNIIA
Start date: April 17, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effectiveness and cost-effectiveness of contralateral surgical exploration during unilateral inguinal hernia repair in children younger than six months with a unilateral inguinal hernia. In half of the participants contralateral exploration will be performed, while in the other half only unilateral inguinal hernia repair will be performed.