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Hernia clinical trials

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NCT ID: NCT02587403 Completed - Ventral Hernia Clinical Trials

A Comparison of Fortiva and Strattice Tissue Matrices in Complex, Ventral Hernia Repair

Start date: December 2, 2015
Phase: N/A
Study type: Interventional

The objective of this study is to compare the effectiveness of Fortiva Porcine Dermis versus Strattice Reconstructive Tissue Matrix for the underlay reinforcement of complex ventral hernia repair and assess post-operative complication rates, long term hernia recurrence rates.

NCT ID: NCT02576184 Completed - Clinical trials for Incisional Hernia After Diverting Stoma Closure

Mesh Reinforcement During Temporary Stoma Closure After Sphincter-Saving Rectal Cancer Surgery

MEMBO
Start date: December 2015
Phase: N/A
Study type: Interventional

This study aim to assess long-term results of an incisional hernia-prophylactic mesh placement during stoma reversal after total mesorectal excision (TME) for rectal cancer

NCT ID: NCT02572622 Completed - Clinical trials for Lumbar Disc Herniation

Comparison of Different Treatment Methods in Lumbal Disc Herniation Treatment

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

The aim of this study is to determine the effectiveness of three different treatment methods which consists spinal decompression, deep friction massage and exercise. The patients were separated three groups Group one received non-surgical spinal decompression therapy, group two received non-surgical spinal decompression, lumbar stabilization exercises and manual therapy, group three received manual therapy and lumbar stabilization exercises. All groups completed 15 sessions of therapy. In each session, pain severity was assessed with numeric analog scale, straight leg raise test applied and the degree of the hip flexion where the patient reported pain were recorded, respectively. Static, dynamic muscle strength-endurance tests were applied before the treatment sessions started, after the treatment sessions ended, six weeks after and three months after the study. Oswestry Disability Scale (ODI), Back Performance Scale (BPS), Lanss Neuropathic pain Questionnaire, Fear-Avoidance-Beliefs Questionnaire (FABQ) and McGill Pain Questionnaire were applied before the treatment sessions started, after the treatment sessions ended and three months after the study. Gradient of disc height and thickness of the herniation were assessed segmentally with magnetic resonance imagination (MRI) before the study and three months after the study.

NCT ID: NCT02564757 Completed - Clinical trials for Recurrent Hernia of Anterior Abdominal Wall

Does Pregnancy Increase Risk of Ventral Hernia Recurrence?

Start date: September 2015
Phase: N/A
Study type: Observational

The investigators will examine if pregnancy increases risk of ventral hernia recurrence

NCT ID: NCT02561910 Completed - Clinical trials for Unilateral Inguinal Hernia With Gangrene and Obstruction

Effectivity of Laparoscopic Inguinal Hernia Repair (TAPP) in Daily Clinical Practice - Early and Long-term Results

Start date: January 2000
Phase: N/A
Study type: Observational

The effectiveness of laparoscopic inguinal hernia repair still remains unclear. During a one year period a total of 1208 inguinal hernias in 952 patients were consecutively operated using the laparoscopic technique by a total of 11 general surgeons in daily clinical routine. Laparoscopic hernia repair in the TAPP technique seems to have the potential to become the standard procedure in inguinal hernia repair in future.

NCT ID: NCT02559102 Completed - Clinical trials for Neurodevelopmental Disorder

Dexmedetomidine Sedation Versus General Anaesthesia for Inguinal Hernia Surgery in Infants

DEGA
Start date: July 2015
Phase: Phase 3
Study type: Interventional

This is a prospective randomized controlled trial comparing dexmedetomidine sedation with caudal anaesthesia, and general sevoflurane anaesthesia with caudal anaesthesia for inguinal herniotomies in neonates and infants below 3 months of age. The investigators will compare the efficacy and adverse events associated with each of these techniques and neurodevelopmental outcomes of the infants in each group at 6 months and 2 years of age.

NCT ID: NCT02537860 Completed - Clinical trials for Inguinal Hernia Repair

Paravertebral Block for Inguinal Hernia Repair in Elderly

Start date: December 2015
Phase: N/A
Study type: Interventional

This prospective double-blinded clinical trial is intended to compare three nerve stimulator- guided paravertebral block injections versus five injections for elderly patients undergoing hernia repair regarding intraoperative hemodynamic stability and postoperative pain.

NCT ID: NCT02527083 Completed - Chronic Pain Clinical Trials

Influence of Anesthetic Technique on Acute and Chronic Neuropathic Pain

Start date: January 2015
Phase: Phase 4
Study type: Interventional

Research suggests that the type of anesthesia used for surgery may affect intraoperative stress hormone levels. There is also data to support that an increased level of stress hormones leads to increased pain after surgery. The primary aim of this study is to determine the effect of anesthesia type on long term pain after hernia surgery. In this study, patients undergoing inguinal hernia repair will be randomized to an anesthetic group, either Total Intravenous Anesthesia (TIVA) maintained with propofol or Balanced Inhaled Anesthesia (BIA) maintained with sevoflurane. This will allow us to look at any differences in short and long-term pain after hernia repair depending on type of anesthesia received.

NCT ID: NCT02525666 Completed - Quality of Life Clinical Trials

Bilateral Laparoscopic Repair of Groin Hernias With One Large Self-fixating Mesh (ProGripTM)

BigWig
Start date: August 2015
Phase:
Study type: Observational

Investigation of a bilateral inguinal hernia repair using one large self-fixating mesh covering both groins. Health outcomes are assessed using different questionaires with focus on urinary symptoms (with ICIQ-MLUTS score), the recurrence rate, postoperative pain measurement, and Quality of Life assessment with EuraHS-QoL and chronic pain monitoring for 12 months.

NCT ID: NCT02466451 Completed - Clinical trials for Diaphragmatic Hernia

Study in Children With the Diagnosis of Congenital Diaphragmatic Hernia (CDH) and Oesophageal Atresia (EA)

CDH-EA
Start date: March 2014
Phase: N/A
Study type: Observational

Observational longitudinal study in children operated at birth on diaphragmatic hernia and/or oesophageal atresia : assessment of lung function parameters; assessment of quality of life and cognitive development; assessment of stress parenting and strategies of adaptation.