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Hernia, Inguinal clinical trials

View clinical trials related to Hernia, Inguinal.

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NCT ID: NCT02932033 Not yet recruiting - Inguinal Hernia Clinical Trials

Trial Comparing Tack Versus Histoacryl Mesh Fixation After Endoscopic TEP(Total Extraperitoneal) Repair for Bilateral Inguinal Hernia

TEP
Start date: November 2016
Phase: N/A
Study type: Interventional

This prospective randomized trial is performed to analyze the post-operative pain (acute and chronic) after endoscopic TEP repair after bilateral inguinal hernia repair.

NCT ID: NCT02928146 Not yet recruiting - Inguinal Hernia Clinical Trials

Lichtenstein Versus TAPP and TEP in Groin Hernioplasty

TAPP&TEP
Start date: January 2017
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the effectiveness of various methods of inguinal hernia repair and to evaluate techniques of synthetic mesh fixation during laparoscopic and open hernia repair.

NCT ID: NCT02788812 Not yet recruiting - Inguinal Hernia Clinical Trials

QOL in Incarcerated Inguinal Hernias: TAPP Vs Open Repair

Start date: June 2016
Phase: N/A
Study type: Interventional

To determine if there is a difference in the quality of life in between patients who undergoes laparoscopic transabdominal pre-peritoneal (TAPP) or modified Lichtenstein hernioplasty

NCT ID: NCT02723045 Not yet recruiting - Inguinal Hernia Clinical Trials

Quality of Life of TEP vs Lichtenstein Hernioplasty

Start date: April 2016
Phase: N/A
Study type: Interventional

To determine if there is a difference in the quality of life in between patients who undergoes laparoscopic totally extra-peritoneal (TEP) or modified Lichtenstein hernioplasty

NCT ID: NCT02646722 Not yet recruiting - Inguinal Hernia Clinical Trials

Relation Between Withdrawal Movement for Rocuronium and Emergence Agitation

Start date: January 2016
Phase: N/A
Study type: Observational

Rocuronium results in burning pain on injection site. It can be reduced by local anesthetics or opioid, but still some patients, especially in children, show withdrawal movement for pain. This might resulted from individual pain sensitivity. Emergence agitation (EA) in children is quite frequent postoperatively and is known to be associated with postoperative pain. If a patient is susceptible to postoperative pain, he or she would have high probability of EA postoperatively. Therefore, the investigators explore the relation of withdrawal movement of rocuronium and EA.

NCT ID: NCT02646709 Not yet recruiting - Inguinal Hernia Clinical Trials

The Effect of Different Dose of Ketamine With Low Dose Rocuronium in Children

Start date: January 2016
Phase: Phase 4
Study type: Interventional

Rocuronium is suitable for rapid induction within 60-90 seconds and its effect last 24-40 minute after single bolus injection. For outpatient surgery with short operation time, low dose rocuronium is frequently used for rapid recovery at the expense of compromised intubating condition. For better intubating condition, ketamine can be used. However, appropriate dose of ketamine with low dose rocuronium is not established yet. This study, 3 different doses of ketamine with low dose rocuronium will be compared for appropriate intubating condition.

NCT ID: NCT02634255 Not yet recruiting - Inguinal Hernia Clinical Trials

The Onset Time of Rocuronium in Emergency and Elective Surgery

Start date: December 2015
Phase: Phase 3
Study type: Interventional

Rocuronium, a nondepolarizing neuromuscular blocking agent, is used in general anesthesia to provide conditions for endotracheal intubating. Recommended dose is 0,6 mg/kg and 90 seconds after intravenous injection, patients can be intubated. Anxiety levels may vary in patients undergoing emergency and elective surgery. Patients undergoing emergency surgery may display exaggerated laryngoscopic responses. The purpose of this study is to investigate the effect of patient anxiety levels on the onset time of rocuronium in terms of anxiety scores and train of four (TOF) 0.1 times.

NCT ID: NCT02292095 Not yet recruiting - Inguinal Hernia Clinical Trials

Effects of Transverse Abdominis Plane Block Guided by Ultrasound on the Postoperative Analgesia and Quality of Lives Among the Patients Undergo Inguinal Hernia Repair

Start date: January 2016
Phase: Phase 4
Study type: Interventional

The incidence of post-operative pain after open inguinal hernia repair is high and impair the quality of lives of the patients.The purpose of this study is to determine whether transverse abdominis plane block combined with intravenous patient controlled analgesia is superior to intravenous patient controlled analgesia in improving the quality of life and reducing the incidence of chronic post-surgical pain

NCT ID: NCT01860469 Not yet recruiting - Clinical trials for Patients Undergoing Ventral or Inguinal Hernia Repair

Reducing Mesh Infections in Open Hernia Repairs

Start date: June 2013
Phase: Phase 2/Phase 3
Study type: Interventional

Soaking meshes in a vancomycin solution just prior to their use in open hernia repairs will decrease rates of mesh infection

NCT ID: NCT01069055 Not yet recruiting - Postoperative Pain Clinical Trials

Comparison of Lornoxicam and Paracetamol for Pre-emptive Intravenous Analgesia for Elective Inguinal Hernia Repair

Start date: February 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether lornoxicam or paracetamol is more effective in providing pre-emptive analgesia for adult patients undergoing elective unilateral inguinal hernia repair under general anesthesia.