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Hernia clinical trials

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NCT ID: NCT06179472 Not yet recruiting - Clinical trials for Congenital Diaphragmatic Hernia

Fetoscopic Endoluminal Tracheal Occlusion for Severe Left and Right Congenital Diaphragmatic Hernia

Start date: January 15, 2025
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the feasibility and efficacy of performing Fetoscopic Endoluminal Tracheal Occlusion (FETO) surgery and removal of the BALT Goldbal2 balloon at the UW Health Fetal Diagnosis and Treatment Center which resides in UnityPoint Health-Meriter (UPH-Meriter) hospital as well as the American Family Children's Hospital (AFCH). We hypothesize that FETO balloon placement and removal can be performed safely at our institution and may increase survival and decrease morbidity when compared to standard prenatal care for the treatment of severe left or right congenital diaphragmatic hernia (CDH).

NCT ID: NCT06165133 Not yet recruiting - Inguinal Hernia Clinical Trials

Task Sharing in InGuinal hErnia Repair Between Surgeons and Non-surgeon Physicians

TIGER
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

TIGER is a multicentre, 2-arm, parallel group, assessor blinded, non-inferiority randomised controlled trial with an internal pilot to assess if non-surgeon physicians (NSPs) can effectively perform mesh inguinal hernia repair compared to fully trained surgeons in adult patients with non-complicated inguinal hernia.

NCT ID: NCT06155851 Not yet recruiting - Hiatus Hernia Clinical Trials

Prevalence of Hiatus Hernia in Gastro-Esophageal Reflux Disease Patients Underwent Upper Endoscopy

Start date: December 1, 2023
Phase:
Study type: Observational

To study the prevalence of hiatus hernia in GERD patients underwent upper endoscopy To study the effect of hiatus hernia on the severity of GERD symptoms.

NCT ID: NCT06155253 Not yet recruiting - Hernia, Inguinal Clinical Trials

Comparing Bi-level and Single-level ESP Block for Open Inguinal Hernia Repair

Start date: December 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the effects of single-level and bi-level erector spinae plane block in open inguinal hernia repair surgery. The main question it aims to answer are: - Whether bi-level ESP block will improve pain control after open inguinal hernia repair surgery - Whether bi-level ESP block will improve quality of recovery after open inguinal hernia repair surgery Participants will receive erector spinae plane block, and will be randomised into 2 groups, single-level ESP block and bi-level ESP block, before open hernia repair surgery. They will be followed up after operation for assessment of pain control and quality of recovery.

NCT ID: NCT06152770 Not yet recruiting - Pediatric Hernia Clinical Trials

Comparison of Turkish Children's Actual Weights With Which Predicted Weights by Estimation Methods

CTCAWPWM
Start date: December 1, 2023
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to compare body weigth with the prediceted weigth values abtracted by weigth estimation methods in Turkish Children. The main question it aims to answer is: to evaluate the suitability of APLS, Luscombe & Owens, Best Guess, Nelson Formula and Broselow Band methods in estimating actual measurements in patients coming to the surgery outpatient clinic of our hospital

NCT ID: NCT06096402 Not yet recruiting - Clinical trials for Paraesophageal Hernia

Gastropexy as a Treatment Option for Paraesophageal Hernia

Start date: June 1, 2024
Phase:
Study type: Observational

The present proposal aims to asses which is the optimal treatment strategy in a clinical study in patients with paraoesophageal hernia (PEH), a condition often found in elderly, fragile patients The investigator want to study the optimal approach to a paraoesophageal hernia (PEH) repair. The incidence of PEH increases with age and the older patient typically has additional co-morbidities, reduced physiological fitness, and frailty which makes surgery challenging regarding increased morbidity and mortality. Thus, the decision to offer surgery can be challenging in this cohort of patients. The need of an anti-reflux procedure as part of the repair is one of the main subjects for discussion worldwide. To date no consensus exists and many surgical centres do a routine anti-reflux procedure as part of their standard operation for PEH. But is this procedure redundant? Can the patients be managed with a less complicated procedure; an anterior gastropexy with comparable outcome?

NCT ID: NCT06077318 Not yet recruiting - Parastomal Hernia Clinical Trials

Comparison of the Sugarbaker and Keyhole Repair for Parastomal Hernia

Start date: October 20, 2023
Phase:
Study type: Observational

Parastomal hernia (PSH) is difficult to manage, with high rates of post-operative recurrence and complication. Keyhole and Sugarbaker are the most commonly used techniques in the surgical repair of the PSH. However, the efficacy and safety of the two surgical methods have not been adequately compared in the East Asian population. Patients diagnosed with PSH who underwent Sugarbaker or Keyhole repair from August 2012 to August 2022 will be included. Patient demographic data and postoperative outcomes will be retrospectively analyzed. The primary outcome measure is the recurrence rate at one year follow-up time.

NCT ID: NCT06060951 Not yet recruiting - Clinical trials for Kidney Failure, Chronic

Relating Abdominal Complications With Peritoneal Pressure Estimation and Reporting

RAPPER
Start date: October 1, 2023
Phase:
Study type: Observational

This is a prospective observational study in people treated with peritoneal dialysis for kidney failure to investigate whether estimated intraperitoneal pressure (eIPP) is correlated with non-infectious PD-related complications in end-stage renal failure patients. It looks to understand how both peritoneal dialysis complications (including fluid leaks and hernias) along with gastrointestinal symptoms are associated with eIPP in people treated with PD.

NCT ID: NCT05999565 Not yet recruiting - Neck Pain Clinical Trials

Investigation of the Effect of Motor Imagery Training in Individuals With Cervical Discogenic Pain

Start date: January 4, 2024
Phase: N/A
Study type: Interventional

In this study, motor control exercises including cervical region, upper extremity and scapular region muscles will be applied routinely in individuals with chronic neck pain. The application will been investigating, called motor imagery training, will been carried out together with motor control exercises.

NCT ID: NCT05994248 Not yet recruiting - Umbilical Hernia Clinical Trials

Randomized Controlled Trial (RCT) Umbilical Hernia Repair (UHR) Absorbable vs Non-absorbable Synthetic Mesh

Start date: September 2024
Phase: N/A
Study type: Interventional

The goal of this study is to see which of two types of mesh is better for fixing an umbilical hernia. One type of mesh is an absorbable synthetic mesh, which goes away on its own in the body, and the other type of mesh is a non-absorbable mesh, which stays in the body forever. The researchers will check if the hernia comes back, how it affects the patient's quality of life, and if there are any problems after the surgery during a three-year period.