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Awake Caudal Catheter Infusion Versus General Anesthesia

Primary Purpose

Inguinal Hernia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Bupivacaine and epinephrine infusion
Sponsored by
Nemours Children's Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inguinal Hernia

Eligibility Criteria

23 Weeks - 60 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Preterm infants less than 60 weeks post gestational age born at less than 37 weeks gestational age. Patients in the NICU will meet discharge criteria with or without supplemental oxygen prior to surgical scheduling for inguinal hernia repair. Exclusion Criteria: Patient undergoing other invasive procedures (i.e. gastrostomy tube placement, tracheostomy, laser eye treatment) Medical condition that would prevent a regional anesthetic from being performed (i.e. bleeding diathesis, vertebral anomalies, and spinal cord injury prior to surgery) Contradictions to the prescribed medications in the protocol.

Sites / Locations

  • Nemours Children's Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

The Caudal Infusion Group

The General Anesthesia Group

Arm Description

Continuous caudal infusion.

Single caudal injection with general anesthesia.

Outcomes

Primary Outcome Measures

The time it takes to return to baseline respiratory function.
Success of surgical completion.
Number of apneic episodes.
Cessation of breathing by a premature infant that lasts for more than 20 seconds and/or is accompanied by hypoxia or bradycardia.
Number of bradycardia events.
heart rate <90.

Secondary Outcome Measures

Decrease days to hospital discharge.
Decreased number of post-operative narcotics used per day.
Decreased operative time.
Decreased days of mechanical ventilation.
Decreased time to full feeds.

Full Information

First Posted
June 16, 2023
Last Updated
June 16, 2023
Sponsor
Nemours Children's Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT05919732
Brief Title
Awake Caudal Catheter Infusion Versus General Anesthesia
Official Title
Awake Caudal Catheter Infusion Versus General Anesthesia and Single-dose Caudal Injection for Preterm NICU Patients Undergoing Inguinal Herniorraphy.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
March 8, 2016 (Actual)
Primary Completion Date
March 8, 2018 (Actual)
Study Completion Date
March 8, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nemours Children's Clinic

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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).
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inguinal Hernia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
A prospective, blinded, randomized controlled trial
Masking
ParticipantCare Provider
Masking Description
The statistician for the study will generate a randomization table. An unblinded research coordinator will prepare randomization envelopes which will be numbered sequentially and placed in a bin located in the secure medication room in the peri-operative suite.Intra-operatively, neither the anesthesiologist nor the surgeon will be blinded since they are present from the induction of anesthesia until the conclusion of the operation for patient safety. The doctors, nurses and others caring for the infant postoperatively will be blinded.
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
The Caudal Infusion Group
Arm Type
Experimental
Arm Description
Continuous caudal infusion.
Arm Title
The General Anesthesia Group
Arm Type
Active Comparator
Arm Description
Single caudal injection with general anesthesia.
Intervention Type
Drug
Intervention Name(s)
Bupivacaine and epinephrine infusion
Intervention Description
For caudal infusion group: bupivacaine .3% + 1: 200,000 epinephrine (dose 3mg/kg) will be administered via the catheter. For general anesthesia group: bupivacaine 0.25% + 1:200,000 epinephrine (total dose 2.5mg/kg) prior to start of the surgery.
Primary Outcome Measure Information:
Title
The time it takes to return to baseline respiratory function.
Time Frame
24 hours post operative
Title
Success of surgical completion.
Time Frame
24 hours post operative
Title
Number of apneic episodes.
Description
Cessation of breathing by a premature infant that lasts for more than 20 seconds and/or is accompanied by hypoxia or bradycardia.
Time Frame
24 hours post operative
Title
Number of bradycardia events.
Description
heart rate <90.
Time Frame
24 hours post operative
Secondary Outcome Measure Information:
Title
Decrease days to hospital discharge.
Time Frame
24 hours post operative
Title
Decreased number of post-operative narcotics used per day.
Time Frame
24 hours post operative
Title
Decreased operative time.
Time Frame
24 hours post operative
Title
Decreased days of mechanical ventilation.
Time Frame
24 hours post operative
Title
Decreased time to full feeds.
Time Frame
24 hours post operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
23 Weeks
Maximum Age & Unit of Time
60 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Preterm infants less than 60 weeks post gestational age born at less than 37 weeks gestational age. Patients in the NICU will meet discharge criteria with or without supplemental oxygen prior to surgical scheduling for inguinal hernia repair. Exclusion Criteria: Patient undergoing other invasive procedures (i.e. gastrostomy tube placement, tracheostomy, laser eye treatment) Medical condition that would prevent a regional anesthetic from being performed (i.e. bleeding diathesis, vertebral anomalies, and spinal cord injury prior to surgery) Contradictions to the prescribed medications in the protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert B Bryskin, MD
Organizational Affiliation
Nemours Children's Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Children's Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes

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Awake Caudal Catheter Infusion Versus General Anesthesia

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