Inguinal Hernia Clinical Trial
Official title:
Awake Caudal Catheter Infusion Versus General Anesthesia and Single-dose Caudal Injection for Preterm Neonatal Intensive Care Unit (NICU) Patients Undergoing Inguinal Herniorrhaphy.
It is well established that preterm inguinal hernias discovered in the NICU pose a significant surgical risk due to the associated co-morbid conditions that accompany these patients. Currently, the standard of care in the United States is general anesthesia. There have been studies that have established that elective outpatient repair of inguinal hernias found in the NICU can be safely performed. Patients that are ready for discharge from the NICU will have inguinal hernia repair prior to leaving. Inguinal hernia repair will also be done on those premature infants that are seen in the Nemours surgical clinic. Spinal anesthesia is currently the most common anesthetic procedure used in the surgical treatment of preterm inguinal hernias after general anesthesia. Caudal catheter technique has been proven to safely provide post-operative care of premature infants. The caudal catheter technique involves placement of a small catheter under ultrasound guidance into the caudal epidural canal to allow re-dosing of local anesthetic during the case and has been shown to be safe and effective management in neonates (Somri M, 2007).
This is a prospective, blinded, randomized controlled trial evaluating the effectiveness of awake caudal catheter infusion versus single dose caudal injection and general anesthesia in the surgical management of preterm infant inguinal hernia repair. Spinal anesthesia has been advocated for but highly rejected in the pediatric surgical community due to its high failure rate, which can be up to 28%. Spinal anesthesia is a form of regional anesthesia involving injection of a local anesthetic into the subarachnoid space, via a fine needle, in a single injection. The failure rate has to do with the time constraint of spinal anesthesia, which is approximately 1 hour. It is difficult to perform a bilateral inguinal hernia in that time duration, necessitating a return trip to the operating room for the contralateral side or intubation midway through the surgical case. An alternative to spinal anesthesia that results in an ability to sustain regional anesthetic effect for a longer duration is the caudal catheter infusion. We hypothesize that awake caudal catheter infusion will allow for the following benefits (1) greater than 2 hour anesthetic time via re-dosing which will allow for the completion of the planned surgical procedure (2) exhibit a negligible failure rate (3) minimize post-operative complications that have been associated with general anesthesia in the preterm neonate. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03023462 -
Efficacy of an Anterior Quadratus Lumborum Block vs. a TAP-block for Inguinal Hernia Repair
|
N/A | |
Completed |
NCT04272320 -
The Efficacy of Transversalis Fascia Plane Block in Pediatric Inguinal Hernia Repair
|
N/A | |
Recruiting |
NCT03904888 -
Conventional Versus Robot Assisted Laparoscopic Inguinal Hernia Repair
|
N/A | |
Recruiting |
NCT03856710 -
Self Fixating Versus Stapled Mesh for Laparoscopic Inguinal Hernia Repair
|
N/A | |
Completed |
NCT02240550 -
A Comparative Clinical Study to Evaluate the Effectiveness of ProFlor vs. Lichtenstein for Inguinal Hernia Repair
|
N/A | |
Completed |
NCT01679353 -
Comparison of Analgesic Effect of Magnesium Added to Ropivacaine and Ropivacaine Alone in Caudal Analgesia on Postoperative Pain Control in Pediatric Patients Undergoing Inguinal Hernia Repair
|
N/A | |
Completed |
NCT01943760 -
Tamadol Wound Infiltration in Children Under Inguinal Hernioplasty
|
Phase 4 | |
Recruiting |
NCT01450345 -
Efficacy of Pre-operative Oral Pregabalin in Ambulatory Inguinal Hernia Repair for Post Operative Pain
|
Phase 3 | |
Active, not recruiting |
NCT00968773 -
Rebound Hernia Repair Device Mesh Trial
|
Phase 4 | |
Completed |
NCT01000116 -
Fibrin Glue Versus Tacked Fixation in Groin Hernia Repair (TAPP)
|
N/A | |
Completed |
NCT01117337 -
Comparing Non-fixation of Mesh to Mesh Fixation in Laparoscopic Inguinal Hernia Repair
|
Phase 4 | |
Terminated |
NCT00226161 -
Chronic Pain After Inguinal Herniorrhaphy
|
N/A | |
Completed |
NCT05837013 -
Open and Laparoscopic Total Extraperitoneal Repair Under Spinal Anesthesia Versus General Anesthesia
|
N/A | |
Recruiting |
NCT05058378 -
Correlation Between Spinal Anesthesia and Perfusion Index
|
||
Completed |
NCT01637818 -
Long-term Follow-up of Lichtenstein's Operation Versus Mesh Plug Repair
|
N/A | |
Recruiting |
NCT05879770 -
Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?
|
||
Completed |
NCT05159232 -
Length of Hospital Stay in Laparoscopic Transabdominal Preperitoneal Vs. Open Mesh Repair in Inguinal Hernia: A Randomised Controlled Trial
|
N/A | |
Completed |
NCT05107986 -
Laparoscopy in Complicated Groin Hernia
|
||
Active, not recruiting |
NCT04328597 -
Portuguese Inguinal Hernia Cohort (PINE) Study
|
||
Completed |
NCT04033055 -
Antalgic Efficacy of CycloMeshâ„¢ Soaked in Ropivacaine Hydrochloride in Uncomplicated Inguinal Hernia.
|
N/A |