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Hernia clinical trials

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NCT ID: NCT05003726 Completed - Clinical trials for Lumbar Disc Herniation

Non-pharmacological Treatment and Pharmacological Treatment for Non-acute Lumbar Disc Herniation

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

This study is a 2-armed parallel, multi-centered, pragmatic clinical trial that compares the comparative effectiveness of non-pharmacological treatment and pharmacological treatment for non-acute lumbar disc herniation.

NCT ID: NCT04998929 Completed - Navel; Hernia Clinical Trials

A Common But Unknown Disease; Nave Sliding (NS)

NS
Start date: August 1, 2020
Phase:
Study type: Observational

The present study is a case series study, conducted to introduce a common disease of abdominal wall which has received less attention in scientific resources. The study population was all patients who following repeated hospital visits did not improve, and for their last try, they visited a traditional clinic, and were diagnosed with umbilical hernia.

NCT ID: NCT04981301 Completed - Clinical trials for Lumbar Disc Herniation

Quadratus Lumborum Block for Lumbar Spinal Surgery

Start date: August 2, 2021
Phase: N/A
Study type: Interventional

Spine surgery in thoracolumbar region is one of the most common surgeries performed for the treatment of leg and back pain. Pain management is especially important for these patients since chronic pain often occurs after surgery. Severe pain may occur at postoperative period in patients following lumbar disc herniation (LDH) operation. Postoperative effective pain treatment provides early mobilization and shorter hospital stay, thus complications due to hospitalization such as infection and thromboembolism may be reduced. Ultrasound-guided quadratus lumborum block (QLB) is a fascial plane block where local anesthetic is injected adjacent to the quadratus lumborum muscle with the goal of anesthetizing the thoracolumbar nerves. The aim of this study is to evaluate the efficacy of US-guided QLB for postoperative analgesia management after lumbar disc herniation-laminectomy surgery. The primary aim is to evaluate postoperative pain scores (VAS), the secondary aim is to evaluate use of rescue analgesia and adverse effects (allergic reaction, nausea, vomiting).

NCT ID: NCT04961346 Completed - Incisional Hernia Clinical Trials

RCT Comparing Lightweight vs. Heavyweight Meshes in Incisional Hernia Repair

Start date: September 2004
Phase: N/A
Study type: Interventional

In this randomized, controlled, prospective multicentre clinical trial with a parallel group design a large-pore, lightweight polypropylene mesh (Ultrapro®) is compared to a small-pore, heavyweight polypropylene mesh (Premilene®), within a standardized, retromuscular mesh augmentation to identify the superiority of the lightweight mesh. Included patients are examined at five scheduled follow-up visits (5 and 21 days, 4, 12 and 24 months after surgery). The primary outcome criterion is foreign body sensation 12 month after surgery. Further secondary endpoint criteria are the occurrence of haematoma or haematoma requiring surgery at the 5-day visit, seroma, wound infection, and chronic pain within 24 months postoperatively. Quality of life was investigated by the SF-36®.

NCT ID: NCT04947202 Completed - Ventral Hernia Clinical Trials

Clinical Study on the Safety of SAFIL® MESH

SAFIL_MESH
Start date: July 1, 2021
Phase:
Study type: Observational

Observational, Retrospective, Multi-center Clinical Study on the Safety of SAFIL® MESH in Patients Undergoing Reinforcement of Soft Tissues After Abdominal Wall Surgery or Other Fascial Defects

NCT ID: NCT04941170 Completed - Pain Clinical Trials

U/s Guided Oblique Subcostal Transversus Abdominis Plane Block Versus Erector Spinae Plane Block as Preemptive Analgesia

Start date: June 29, 2021
Phase: Phase 4
Study type: Interventional

Administration of opioids for the treatment of acute pain after open umbilical hernia repair is associated with many side effects. Erector spinae plane (ESP) block is a novel inter-fascial plane block used in postoperative pain and chronic neuropathic pain relief of the thoracoabdominal region.TAP block is a regional injection of local anaesthetic between the transversus abdominis and internal oblique muscle planes. TAP block affects the sensory nerves of the anterolateral abdominal wall (T6-L1) that innervate the abdomen.

NCT ID: NCT04930523 Completed - Clinical trials for Lumbar Disc Herniation

Effect of Decompression With and Without ELDOA in Lumber Disc Protrusion Patients

ELDOA
Start date: June 11, 2021
Phase: N/A
Study type: Interventional

The study will be conducted to determine the effects of spinal decompression with and without ELDOA in patients of lumbar disc protrusion. A total of twenty patient with lumber disc protrusion will be taken after fulfilling the inclusion criteria. the patient will be divided in experimental group i.e. ELDOA along with decompression and control group. Both session got pre and post session along with general low back exs.home plan along with precautions was guided to every patient of control and experimental group.NPRS ,ODI is assess in first and fourth session. The data will be analyzed through IBM SPSS version 21.

NCT ID: NCT04900649 Completed - Clinical trials for Hernias, Diaphragmatic, Congenital

Resistance Exercise in Children With Post-operative Congenital Diaphragmatic Hernia

hernia
Start date: May 1, 2020
Phase: N/A
Study type: Interventional

Congenital diaphragmatic hernia (CDH) is a life-threatening condition with long-term complications including respiratory tract infections, respiratory muscle weakness, and abnormal lung functions. This study, therefore, has been designed to ascertain the effect of chest resistance exercise and chest expansion exercise on respiratory muscle strength, lung function, and chest mobility in children with post-operative CDH.

NCT ID: NCT04891601 Completed - Inguinal Hernia Clinical Trials

Mesh Alone VS Combined Mesh and Darn in the Management of Primary Inguinal Hernia in Adult Males

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

A prospective randomized study involved 228 individuals with primary inguinal hernia, operated in our departments, between January 2015 to February 2018. The duration of hospital stay, operative time, duration of returning to routine activities, postsurgical sequels and recurrence rates estimated. We randomly allocated it into two groups: mesh repair was applied to 166 patients (Group 1) and combined both mesh, and darn repair applied to 162 patients (Group 2).

NCT ID: NCT04888078 Completed - Inguinal Hernia Clinical Trials

Bassini Inguinal Hernia Repair: Obsolete Or Still A Viable Surgical Option?

Start date: January 1, 2006
Phase:
Study type: Observational

Retrospective review of hernia surgery patients at HHMcGuire VAMC focusing on repair type and postoperative complications.