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Hernia clinical trials

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NCT ID: NCT04269330 Completed - Inguinal Hernia Clinical Trials

Normal and Small Size Mesh in Open Inguinal Herni Repair

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

Recent years, lots of treatment teqnique have development. We aimed that comparising the normal and small size meshes in the inguinal hernia patients.

NCT ID: NCT04266561 Completed - Congenital Hernia Clinical Trials

Laparoscopic Recurrent Inguinal Hernia Repair

Start date: February 2010
Phase: N/A
Study type: Interventional

Laparoscopic management of recurrent inguinal hernia in children has been recently introduced in surgical practice. One of the most important advantages of using the laparoscopic approach in cases with recurrent inguinal hernia (RIH) is that it avoids the previous operation site thus avoiding injuries to the vas and vessels [19]. Some authors designed a study to compare laparoscopic hernia repairs with classical open repairs for pediatric RIH following the first open repair. They stated that avoiding the scarred tissue the former operation area with the laparoscopic approach facilitates the procedure and decreases both the operative time and complication rate. [5]. Further, it is as simple as a fresh hernia repair because the time taken for the repair of recurrent hernia laparoscopically was the same as the fresh laparoscopic repair with no added complication [5,20]. In laparoscopic surgery, approaching the hernia defect from within the abdomen, makes the area of interest bloodless, and the magnification renders anatomy very clear, making surgery precise [6,7].

NCT ID: NCT04266132 Recruiting - Inguinal Hernia Clinical Trials

Ultrasound Guided Retrolaminar Block for Pediatric Inguinal Hernia

Start date: May 17, 2020
Phase: N/A
Study type: Interventional

Regional analgesia for inguinal hernia repair in children has attracted increasing interest and different techniques like Caudal block, lumbar epidural block, wound infiltration, Ilio-inguinal nerve block and paravertebral block have been used with varying success. Ilio-inguinal nerve blockade has been widely used in this context but the duration of the block is also limited to the early postoperative period. Paravertebral blockade has been shown to produce long lasting postoperative analgesia when used in combination with general anaesthesia in paediatric herniorrhaphy . Ultrasound-guided retrolaminar block is one of the newer and technically simpler alternatives to the traditional PV block . The aim of this study is to test the efficacy and safety of ultrasound guided retrolaminar block(RLB) as an analgesic technique in surgery of pediatric inguinal hernia in comparison with with ilioinguinal nerve block(INB). It is hypothesized that RLB block will provide longer duration of postoperative analgesia than INB with few side effects.

NCT ID: NCT04261673 Recruiting - Craniotomy Clinical Trials

Prospective Randomized Evaluation of Decompressive Ipsilateral Craniectomy for Traumatic Acute Epidural Hematoma

PREDICT-AEDH
Start date: May 23, 2020
Phase: N/A
Study type: Interventional

Although craniotomy provides a more complete evacuation of the acute epidural hematoma, there are insufficient data to support specific surgical treatment method. We aim to perform a multi-center, parallel-group randomized clinical trial to compare the outcome and cost-effectiveness of decompressive craniectomy versus craniotomy for the treatment of traumatic brain injury patients with cerebral herniation undergoing evacuation of an acute epidural hematoma.

NCT ID: NCT04260685 Completed - Clinical trials for Lumbar Disc Herniation

Lidocaine Versus Esmolol for Optimizing Surgical Field Visibility

Start date: February 4, 2020
Phase: Phase 2
Study type: Interventional

Intra-operative blood loss is an important attribution and predictor of the lumbar spine surgery and patient outcome. Stripping the muscle off bone makes more exposed bleeding spine surface is one of causes for blood loss during lumbar surgeries. The importance to decrease the bleeding is to improve the surgical field visibility which provides technical ease for surgeon and decreases the surgical time besides maintaining the hemodynamic stability. In past, there were many trials to minimize surgical blood loss by different drugs such as Na Nitroprusside, magnesium sulfate, volatile anesthetics and beta-adrenergic antagonist.

NCT ID: NCT04254250 Active, not recruiting - Clinical trials for Intervertebral Disc Herniation

Preoperative Estimation Of Disc Herniation Recurrence In Patients With Lumbar Disc Herniation

Start date: February 10, 2020
Phase:
Study type: Observational [Patient Registry]

This study will be conducted at Research Institute of Traumatology and Orthopedics (NRITO) n.a. Ya.L.Tsivyan, Novosibirsk, Russia. The current study is prospective observational study to evaluate the efficacy of preoperative estimation of disc herniation recurrence among patients with lumbar disc herniation using predictive mathematical model at terms 3 years postoperatively . It is expected to enroll 350 patients aged 18-70 with lumbar disc herniation. Risk estimation of disc herniation recurrence will be evaluated preoperatively, then patient will undergo conventional microdiscectomy. Postoperative eximanation will include Visits every 6-months during 3 years to evaluate clinical outcomes.

NCT ID: NCT04254237 Completed - Incisional Hernia Clinical Trials

Trocar Site Hernia After Laparoscopic Cholecystectomy, Supra Versus Infraumbilical Incision for Umbilical Trocar Entry

HOT
Start date: February 6, 2020
Phase: N/A
Study type: Interventional

Trocar site hernia is a specific complication of laparoscopic surgery. The increasingly frequent use of the laparoscopic approach has resulted in an increase in the number of hernias, mainly at the umbilical area. The appearance of a trocar site hernia can cause complications in the short and long term to the patient who may end up needing a reoperation. In this study we want to compare the supraumbilical versus the infraumbilical location of the laparoscopy entry trocar, in terms of incisional hernia incidence.

NCT ID: NCT04235478 Active, not recruiting - Pain, Neuropathic Clinical Trials

Effect of the Cervical Interlaminar Epidural Steroid Injection on Quality of Life, Pain and Disability

Start date: December 27, 2017
Phase: N/A
Study type: Interventional

To evaluate the effect of cervical interlaminar epidural steroid injections on the neuropathic pain, quality of life and disability patients with cervical radiculopathy. After the clinical and MRG evaluations of patients with neck and arm pain, injection was given to eligible patients. Patients undergone the procedure were evaluated before and after injection for neuropathic pain, quality of life and disability.

NCT ID: NCT04231071 Completed - Umbilical Hernia Clinical Trials

Mesh Versus Suture Repair in Umbilical Hernias - A Multicenter Trial

SUMMER
Start date: February 3, 2020
Phase: N/A
Study type: Interventional

Umbilical hernia repair is one of the most common surgical performance in general surgery. Up to now, the use of suture repair has been the preferred technique for small umbilical hernia defects without any gold standard procedure. Mesh have been reserved to larger umbilical hernia defects. However, there is an increasing evidence that mesh reinforcement could be advantageous to lower the high recurrence rates also in smaller umbilical hernias. A remained important question is in what anatomical position the mesh should be placed. The investigators hypothesize that the use of an onlay mesh in small umbilical hernia defects can reduces recurrence rates without increasing postoperative complications compared to a suture repair.

NCT ID: NCT04230733 Completed - Clinical trials for Lumbar Disc Herniation

Pelvis Displacement and Gait Indicators in Patient With Lumbar Disc Herniation

Start date: August 20, 2019
Phase:
Study type: Observational

The purpose of this study is to investigate the correlation between pattern of gait and pelvic displacement in patients with lumbar disc herniation.