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Hernia clinical trials

View clinical trials related to Hernia.

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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: NCT03674372 Recruiting - Clinical trials for Congenital Diaphragmatic Hernia

Fetoscopic Endoluminal Tracheal Occlusion

FETO
Start date: November 16, 2018
Phase: N/A
Study type: Interventional

The purpose of this research study is to see if the FETO surgery and FETO release (surgery to remove the device) works and is safe for babies with severe right or left Congenital Diaphragmatic Hernia (CDH). CDH is a condition in which a hole in the baby's diaphragm allows the abdominal organs to move into the chest and limit lung growth. The goal of the FETO device is to block the airway with a balloon-type device, allowing fluid to build up and help the unborn baby's lungs grow. Bigger lungs may improve the baby's quality of life.

NCT ID: NCT03667287 Recruiting - Parastomal Hernia Clinical Trials

Stoma Hernia Intraperitoneal Full-Thickness Skin

SHIFT
Start date: January 23, 2018
Phase: N/A
Study type: Interventional

This is a prospective randomized study to compare surgical methods for the repair of parastomal hernia.

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: NCT03651440 Completed - Clinical trials for Lumbar Disc Herniation

Effect of PNF and Lumbar Stabilization Exercises on Muscle Strength and Endurance in Lumbar Disc Hernia

PNF
Start date: May 1, 2014
Phase: N/A
Study type: Interventional

Background/Objective: This study investigates the effect of lumbar stabilization and proprioceptive neuromuscular facilitation (PNF) training on muscle strength and muscle endurance. Methods: Sixty-four participants between the ages of 15 and 69 years, graded "protrusion and bulging lumbar herniation" according to the Macnab Classification, were divided into four groups of 16: lumbar stabilization training (strength training, 5 days/week for 4 weeks); PNF training (5 days/week for 4 weeks); physical therapy (hot pack, TENS, ultrasound, 5 days/week for 4 weeks); and control (without any application). Sociodemographic features were recorded and muscle strength tested. Before and after exercise, a visual analog scale (VAS) and Oswestry Disability Index (ODI) were measured by a physical therapist. After 4 weeks, the evaluations were repeated. Results: There were significant increases in muscle strength and muscle endurance in the lumbar stabilization group, who also showed significant improvement in pain intensity at rest and during activity, and in ODI (p<0.05). Similar results were observed in the PNF group (p<0.05), although not to the same extent. Patients undergoing physical therapy showed significant differences only in pain intensity at rest, at activity, and in ODI (p<0.05). Conclusion: Undertaking an appropriate physiotherapy and rehabilitation program aiming to reduce waist circumference of patients with low muscle strength and low muscle endurance will help to increase muscle strength and endurance and reduce pain, and contribute toward the correction of functional disabilities.

NCT ID: NCT03634046 Active, not recruiting - Clinical trials for Chronic Low Back Pain

PTED Versus Radiofrequency Ablation for Lumbar Disc Herniation

PTED
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

Lumbar disc herniation (LDH) is a common and frequently-occurring disease giving rise to low back pain and (or) leg pain. There are about 1.5 million people with LDH-related pain, accounting for 10% of outpatients each year in China. The mechanism of LDH-related pain is that the degeneration causes the protrusion of the intervertebral disc directly to the lower lumbar nerve root or spinal cord, and the chemical stimulation plays a key role in it. Currently, LDH treatments are mainly divided into conservative treatment, surgical treatment and minimally invasive treatment. The minimally invasive technique is a new technology that has been arising in recent years, with small wound, little bleeding and quick recovery. It mainly includes collagenase dissolving, laser decompression, radiofrequency ablation, etc. Intervertebral disc radiofrequency ablation is an early application of minimally invasive technique with a wide range of applications in a long time. The percutaneous transforaminal endoscopic discectomy (PTED) is a new technique, which is applied in clinics with shorter time, and the implementation and efficacy of the technique need to be further discussed. A case-control clinical trial is designed to compare the efficacy and safety of PTED with radiofrequency ablation in the treatment of LDH. Main outcome is Visual Analogue Scale for leg pain, secondary outcomes are Oswestry disability index, quality of life assessment, Burns Depression Checklist, recovery rate, complications, operation time and radiation exposure time, etc. The follow-up time points are 7 days, 1 month, 6 months and 12 months post-operation.

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.

NCT ID: NCT03613350 Completed - Clinical trials for Lower Urinary Tract Symptom in Severe Cystocele Women

Prevalence Rates of USI, BO, DO and Their Clinical and Urodynamic Findings in Women With ≥Stage II Cystocele

Start date: November 1, 2011
Phase:
Study type: Observational

Prevalence rates of urodynamic stress incontinence (USI), bladder oversensitivity (BO) /detrusor overactivity (DO) or both and their related clinical and urodynamic findings in women with ≥ pelvic organ prolapse quantification stage II cystocele are important for clinical consultation. Thus, the aim of this study was to elucidate the above findings and between-group associations.

NCT ID: NCT03613324 Completed - Clinical trials for Bladder Outlet Obstruction and Detrusor Underactivity in Women With Severe Cystocele

BOO and DU and Their Clinical and Urodynamic Findings in Women With ≥Stage II Cystocele

Start date: January 1, 2011
Phase:
Study type: Observational

Prevalence rates of bladder outlet obstruction (BOO) and detrusor underactivity (DU) and their related clinical and urodynamic findings in women with ≥ pelvic organ prolapse quantification stage II cystocele are important for clinical consultation. Thus, the aim of this study was to elucidate the above findings and between-group associations.

NCT ID: NCT03613311 Completed - Clinical trials for Urodynamic Stress Incontinence in Severe Cystocele Women

Evident, Occult and no Demonstrated USI and UDS Findings in Women With ≥Stage II Cystocele

Start date: November 1, 2011
Phase:
Study type: Observational

Prevalence rates of urodynamic urinary incontinence (USI) subtypes and their related clinical and urodynamic findings in women with ≥ pelvic organ prolapse quantification stage II cystocele are important for clinical consultation, especially for occult USI. Misdiagnosis of occult USI before cystocele repair might lead to occurrence of de novo stress urinary incontinence after cystocele repair. Thus, the aim of this study was to elucidate the above findings and between-group associations.