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Hernia clinical trials

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NCT ID: NCT06467279 Not yet recruiting - Children Clinical Trials

Comparing Inhalation and Total Intravenous Anesthesia Methods

Start date: July 15, 2024
Phase:
Study type: Observational

comparison of Anesthesia by Target-Controlled Infusion and Inhalation Methods on Pediatric Patients Undergoing Inguinal Hernia Repair: Effects on Patient Outcomes

NCT ID: NCT06449378 Not yet recruiting - Hernia Clinical Trials

Transorbâ„¢ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral Hernia

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

The purpose of RECOVER is to evaluate the performance and safety of Transorbâ„¢ self-gripping resorbable mesh in high-risk subjects (at least one risk factor impairing wound healing) when used for reinforcement of abdominal wall soft tissues in procedures involving open extraperitoneal ventral hernia repair, in clean (US); and clean and clean-contaminated (Europe) surgical fields (Centers for Disease Control and Prevention (CDC) Classification I and II. Data from this study will primarily be used to support market approval and European post-market clinical follow-up needs. Secondarily, data will be used for product marketing, future product development, and to support market release and maintenance in global geographies.

NCT ID: NCT06449144 Not yet recruiting - Postoperative Pain Clinical Trials

The Effect of Mindfulness Training on Postoperative Pain - A Solomon Four Group Design

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

The goal of this clinical trial is to learn if mindfulness education works to reduce pain after inguinal hernia operation in adults. The main questions it aims to answer are: Does mindfulness education reduce the pain level after inguinal hernia operation? Does mindfulness education reduce the pain intrusion level after inguinal hernia operation? Does mindfulness education reduce the fear of pain level after inguinal hernia operation? Participants will: Pain level, pain intrusion and fear of pain levels will be determined 24 hours before surgery. Awareness training will be given before surgery. Pain level, pain intrusion and fear of pain levels will be determined 24 hours after surgery.

NCT ID: NCT06444347 Not yet recruiting - Hiatal Hernia Clinical Trials

Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair

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

The aim of this study is to find out if using a certain kind of mesh can reduce the chances of hiatal hernias coming back after anti-reflux surgery. Participants undergoing antireflux surgery will be assigned to one of two groups, a group that has surgery with mesh, or a group that has surgery without mesh.

NCT ID: NCT06426225 Not yet recruiting - General Anesthesia Clinical Trials

Spinal Or General Anesthesia For Umblical Hernia Surgery

Start date: May 15, 2024
Phase: N/A
Study type: Interventional

In this study, the investigators compared spinal anesthesia under ketofol (ketamine-propofol combination) sedation with general anesthesia in terms of intraoperative and postoperative hemodynamics, respiratory parameters and cost in patients undergoing umbilical hernia operation. the investigator aimed to provide the most appropriate and hemodynamically stable option for the patient, to decrease the complication rates and to reduce the associated costs.

NCT ID: NCT06412406 Not yet recruiting - Clinical trials for Paraumbilical Hernia

Comparison Between External Oblique Intercostal Plane Block and the Transversus Abdominis Plane Block in Paraumbilical Hernia Repair as Analgesia for Intraoperative and Postoperative Pain.

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

AIM OF STUDY: Comparison between effect of external oblique intercostal plane block and the Oblique subcostal transversus abdominis plane block in paraumbilical hernia repair as analgesia for intraoperative and postoperative pain.

NCT ID: NCT06367309 Not yet recruiting - Ventral Hernia Clinical Trials

ExtrAperitoneaL Plasty vs Intraperitoneal oNlay mEsh in Ventral Hernia Repair

ALPINE
Start date: May 30, 2024
Phase: N/A
Study type: Interventional

This study investigates on the effect of two different operative techniques to treat abdominal wall hernias. The goal of this clinical trial is to learn if the eTEP (Extended totally extraperitoneal repair) technique leads to a better outcome than the IPOM (Intraperitoneal onlay mesh) technique. The main questions it aims to answer are: - pain after the operation - rate of complications - rate of recurrence and reoperations - quality of life. Participants will: Either be operated using the eTEP or the IPOM technique. Be followed up either in person or via email / phone call at day 1, day 7, day 14, 6 weeks, 6 months, 1, 3 and 5 years after the surgery to asses the above-stated main and some more outcomes.

NCT ID: NCT06364306 Not yet recruiting - Ventral Hernia Clinical Trials

oPen Versus RobotIc retrOmuscular Repair in Medium to Large Ventral Hernias

PRIOR
Start date: June 20, 2024
Phase: N/A
Study type: Interventional

This study investigates on the effect of two different operative techniques to treat large abdominal wall defects. The goal of this clinical trial is to learn if the minimally-invasive, robotically-assisted ventral hernia repair (RVHR) leads to a better outcome than the open ventral hernia repair (OVHR). The main questions it aims to answer are: length of stay after the operation rate of complications rate of recurrence and reoperations quality of life. Participants will: Either be operated using the RVHR or OVHR will be followed up either in person or via email / phone call at day 7, day 30, 6 months, 1, 3 and 5 years after the surgery to asses the above-stated main and some more outcomes.

NCT ID: NCT06352489 Not yet recruiting - Ventral Hernia Clinical Trials

Evaluation of Posterior Component Separation Technique in the Management of Complex Ventral Hernia.

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

- Assess short term outcome of posterior component separation technique(PCS) including the regain of the physiological function of the abdominal wall. - Detect most common post operative complications related to AWR techniques in a 6 months duration after operation.

NCT ID: NCT06317779 Not yet recruiting - Abdominal Disorder Clinical Trials

Evaluation of Laparoscopic Cholecystectomy and Concomitant Paraumbilical Hernia Repair

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

Umbilical hernia frequently accompanies cholelithiasis. It is possible to repair these hernias after completing cholecystectomy.