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Hernia clinical trials

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NCT ID: NCT04329598 Completed - Clinical trials for Lumbar Disc Herniation

Effects of Whole-Body Electromyostimulation Application in Individuals With Lumbar Disc Hernia

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

To determine the effects of WB-EMS application on balance, pain, muscle strength, muscle endurance, flexibility, muscle shortening and quality of life in individuals with Lumbar Disc Hernia and compare it with individuals who have not received this training.

NCT ID: NCT04305509 Completed - Clinical trials for Lumbar Disc Herniation

Outcomes After Chiropractic Spinal Manipulative Therapy With Lumbar Disc Herniation and Radiculopathy

Start date: March 9, 2020
Phase:
Study type: Observational

In a study that was approved nine years ago (EK-22/2009) we could show (i) that spinal manipulative therapy (SMT) is a very effective and safe treatment for acute and chronic lumbar disc herniation (LDH); (ii) that SMT is as effective and less expensive than lumbar nerve root injections and (iii) that the recurrence rate up to one year was very low in acute and in chronic LDH patients. However, the long-term outcome of this conservatively treated LDH patients is unknown. Thus, the objective of this amendment is to investigate the proportion of long-term recurrences in these patients who were treated with SMT for their LDH and to compare these results with already existing data from other treatments, e.g. surgery. This is important information to know whether this conservative method is a sustainable approach for treating LDH.

NCT ID: NCT04303442 Completed - Bleeding Clinical Trials

Corona Mortis in Patients Undergoing TEP for Inguinal Hernia

Start date: January 2, 2020
Phase:
Study type: Observational

This study aim to describe the presence, type and size of Corona mortis (CMOR) in patients undergoing total extraperitoneal (TEP) inguinal hernia repair procedures. This study also aim to describe the preperitoneal vascular anatomy of inguinal area and provide in vivo knowledge about CMOR.

NCT ID: NCT04300153 Completed - Postoperative Pain Clinical Trials

The Effect of Erector Spinae Plane Block on Quality of Recovery and Postoperative Analgesia After Inguinal Hernia Repair

Start date: March 25, 2020
Phase: N/A
Study type: Interventional

Inguinal hernia repair (IHR) is one of the most commonly performed operations in general surgery practice. Different pharmacological approaches and interfascial plane blocks are used to control postoperative pain. Erector spinae plane (ESP) block is a relatively new interfascial plane block which was reported to be effective in different types of surgeries. In this study, the primary aim is to assess the effect of ESP on recovery of patients following open IHR surgery.

NCT ID: NCT04295629 Completed - Clinical trials for Ilioinguinal Nerve Block

The Effects of Ilioinguinal Nerve Block on Chronic Pain in Patients in Inguinal Hernia With Spinal Anesthesia

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Regional anesthesia is a popular anesthetic method in patients who will undergo an inguinal hernia operation. Researchers known that pain in the operating area is a complaint that impairs the quality of life for patients in the long term after the operation. In addition to regional anesthesia, has planned to investigate the effects of applying another drug near the surgery area on pain that may develop in the long term.

NCT ID: NCT04282720 Completed - Hiatal Hernia Clinical Trials

SurgiMend Mesh at the Hiatus

Start date: March 31, 2020
Phase: N/A
Study type: Interventional

Prospective, single-arm, open-label study to evaluate re-occurrence and quality of life in subjects undergoing primary Hiatal hernia repair using SurgiMend biological mesh. Up to 15, with a target of 10, subjects are planned to be enrolled at one site. All subjects will receive the SurgiMend mesh during surgery. Data collected will be compared to historical data. Subjects will complete a pre-operative visit. After surgery, in addition to any standard of care visits, subjects will complete 3- and 6-month follow-ups involving a phone QOL survey and will have an upper GI series at 6 months.

NCT ID: NCT04280094 Completed - Inguinal Hernia Clinical Trials

Can Ideal Mesh Size be Standardized in Open Inguinal Hernia Repair

Start date: June 2, 2020
Phase:
Study type: Observational

Two hundred consecutive unilateral inguinal hernia patients will be included in the study. Patients will be recorded by measuring the distance between the pubic tubercle and the deep inguinal ring, the distance between the inguinal ligament and the internal oblique aponeurosis, the distance between the deep and superficial inguinal ring diameters and their anterior superior iliac spine. The contribution of these measures to the determination of the ideal mesh size will be analyzed.

NCT ID: NCT04272320 Completed - Inguinal Hernia Clinical Trials

The Efficacy of Transversalis Fascia Plane Block in Pediatric Inguinal Hernia Repair

Start date: September 29, 2021
Phase: N/A
Study type: Interventional

In patients undergoing lower abdominal surgery, postoperative pain management is frequently provided with systemic opioids use or neuraxial methods. Ultrasound-guided TFP block is the preferred method to reduce the use of opioids and systemic analgesics for postoperative pain management. TFP block provides anesthesia and analgesia in the inguinal region by blocking the ilioinguinal and iliohypogastric nerves. In this study, we aimed to evaluate the effects of ultrasound-guided TFP Block on postoperative pain scores in pediatric lower abdominal surgery.

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].