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Caudal vs Local Anesthesia in Hypospadias (CLASH)

Primary Purpose

Hypospadias

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Caudal Block Anesthesia
Dorsal Penile Block Anesthesia
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypospadias focused on measuring Hypospadias, Caudal Block, Dorsal Penile Block, Anesthesia, Complications, Post-operative, Urethrocutaneous Fistula, Glans dehiscence

Eligibility Criteria

6 Months - 48 Months (Child)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Males 6-48 months of age at presentation to Pediatric Urology clinics
  • Patient who requires hypospadias repair by fellowship-trained Pediatric Urologists.

Exclusion Criteria:

  • Patients who have undergone previous hypospadias surgery
  • Patients who have contraindications to either caudal or dorsal penile block
  • Inability of parent/guardian to understand English/French
  • Deviation to pre-established anesthesia protocol

Sites / Locations

  • McMaster Children's HospitalRecruiting
  • Children's Hospital, London Health Sciences Centre
  • Children's Hospital of Eastern Ontario
  • The Hospital for Sick Children

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Caudal Block Anesthesia

Dorsal Penile Block Anesthesia

Arm Description

Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine 1mL/kg without epinephrine into the caudal canal, which is the sacral portion of the spinal canal.

Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine without epinephrine into the dorsal portion of the penis.

Outcomes

Primary Outcome Measures

Post-operative Complication Rate
UCF is defined as an abnormal communication between the reconstructed urethra and the skin located between the original meatus and the tip of the penis.Glans dehiscence is considered as a complete separation of the glans wings with or without a band of skin between them.
Recruitment rate
Percentage of eligible participants enrolled, Randomization rate (percentage of enrolled participants randomized)
Protocol violations or Adverse events
Frequency of protocol violations or adverse events related to the study intervention.

Secondary Outcome Measures

Operating Room (OR) time
OR time will be measured in minutes from the time the patient enters the OR to the time surgery is complete
Complications directly related to caudal block
Complications directly related to caudal block include block failure, blood aspiration and intravascular injections.
Complications directly related to dorsal penile block
Complications directly related to dorsal penile block include hematoma and intravascular injection.
Post-operative Pain
Pain scores will be measured through a reliable and validated observer-rated Face, Legs, Activity, Cry, Consolability (FLACC) Behavioural Scale by two trained, blinded, and independent study personnel. Both study personnel will measure pain at admission and discharge during the recovery phase.
Post-operative Pain
Pain scores will be measured through a reliable and validated observer-rated Children's Hospital of Eastern Ontario Pain Scale (CHEOPS) by two trained, blinded, and independent study personnel. Both study personnel will measure pain at admission and discharge during the recovery phase.

Full Information

First Posted
July 27, 2015
Last Updated
March 14, 2023
Sponsor
McMaster University
Collaborators
Canadian Urological Association
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1. Study Identification

Unique Protocol Identification Number
NCT02512887
Brief Title
Caudal vs Local Anesthesia in Hypospadias
Acronym
CLASH
Official Title
Caudal vs Local Anesthesia in Hypospadias: The CLASH Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 2016 (undefined)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Canadian Urological Association

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypospadias is one of the most common congenital malformations of the genitalia in boys, and is typically managed by surgical intervention. During pediatric urological surgery, caudal anesthesia is one of the most common regional anesthetic techniques used. Also known as caudal block, it has been shown to be a safe and effective anesthetic technique in children with a low incidence of anesthesia-related complications.While the reported incidence of complications directly associated with caudal block is low, there is scarce and inconclusive evidence on the impact of caudal anesthesia on the incidence of surgical complications. As a result, the objective of this superiority, randomized controlled trial is to assess whether the use of caudal anesthesia, when compared to dorsal penile block, is associated with a higher rate of urethrocutaneous fistulas and glans dehiscence post hypospadias repair.
Detailed Description
The rationale to conduct a definitive study comes as a result of the limitations inherent in the pre-existing literature due to selection bias, and the primarily retrospective nature of the current evidence, which is unclear whether caudal blocks result in higher complication rates following hypospadias repair. The only way to close this knowledge gap and disturb the current state of clinical equipoise surrounding this topic is to randomly assign the two interventions (caudal or penile block) to patients undergoing hypospadias repair. The rationale to conduct this pilot study is to determine whether the definitive study is feasible and to ensure that any methodological issues are identified and addressed prior to investing significant resources in a definitive trial. This study will be a pilot study to determine the feasibility of conducting a large definitive superiority, parallel, randomized controlled trial (RCT) to assess whether dorsal penile block results in fewer postoperative complications than caudal block in boys (6-48 mos.) undergoing hypospadias repair. Hypospadias repair will be carried out under standardized analgesic administration.. Participants may be given fentanyl (1-3 mcg/kg) at the discretion of the anesthesiologist. Anesthesia will be delivered to all participants via inhalation induction with air/nitrous oxide and sevoflurane. In addition either caudal anesthetic block (0.25% bupivacaine 1 ml/kg to a maximum of 10 ml) or dorsal penile block (bupivacaine without epinephrine 10-20 ml/kg) will be administered based on our randomization scheme. Each patient will also receive antiemetic prophylaxis with dexamethasone 150 mcg/kg ondansetron 50 mcg/kg Acetaminophen suppository 40 mg/kg, and intravenous morphine (0.02-0.1 mg/kg). At Home At home, Oral Morphine (0.2 mg/kg) q4h prn, Ditropan (0.2 mg/kg) q12h prn, Tylenol (15 mg/kg/dose) q4h or Ibuprofen (10 mg/kg/dose) q6h will be prescribed at discharge to be administered at the parents' discretion. Trimethoprim (2 mg/kg) will also be prescribed for administration until catheter removal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypospadias
Keywords
Hypospadias, Caudal Block, Dorsal Penile Block, Anesthesia, Complications, Post-operative, Urethrocutaneous Fistula, Glans dehiscence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
224 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Caudal Block Anesthesia
Arm Type
Experimental
Arm Description
Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine 1mL/kg without epinephrine into the caudal canal, which is the sacral portion of the spinal canal.
Arm Title
Dorsal Penile Block Anesthesia
Arm Type
Active Comparator
Arm Description
Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine without epinephrine into the dorsal portion of the penis.
Intervention Type
Drug
Intervention Name(s)
Caudal Block Anesthesia
Intervention Description
Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine 1mL/kg without epinephrine into the caudal canal, which is the sacral portion of the spinal canal.
Intervention Type
Drug
Intervention Name(s)
Dorsal Penile Block Anesthesia
Other Intervention Name(s)
Local Anesthesia
Intervention Description
Anesthesia will be delivered via inhalation induction with air/nitrous oxide and sevoflurane, and injection of 0.25% bupivacaine without epinephrine into the dorsal portion of the penis.
Primary Outcome Measure Information:
Title
Post-operative Complication Rate
Description
UCF is defined as an abnormal communication between the reconstructed urethra and the skin located between the original meatus and the tip of the penis.Glans dehiscence is considered as a complete separation of the glans wings with or without a band of skin between them.
Time Frame
Follow-up to assess the complications, specifically urethrocutaneous fistula (UCF) and glans dehiscence within 12 months post-surgery.
Title
Recruitment rate
Description
Percentage of eligible participants enrolled, Randomization rate (percentage of enrolled participants randomized)
Time Frame
trial duration 1 year
Title
Protocol violations or Adverse events
Description
Frequency of protocol violations or adverse events related to the study intervention.
Time Frame
trial duration 1 year
Secondary Outcome Measure Information:
Title
Operating Room (OR) time
Description
OR time will be measured in minutes from the time the patient enters the OR to the time surgery is complete
Time Frame
Record duration of operative time (takes on average 30-45 minutes)
Title
Complications directly related to caudal block
Description
Complications directly related to caudal block include block failure, blood aspiration and intravascular injections.
Time Frame
Complications will be measured at a clinic visit 48 hours after surgery.
Title
Complications directly related to dorsal penile block
Description
Complications directly related to dorsal penile block include hematoma and intravascular injection.
Time Frame
Complications will be measured at a clinic visit 48 hours after surgery.
Title
Post-operative Pain
Description
Pain scores will be measured through a reliable and validated observer-rated Face, Legs, Activity, Cry, Consolability (FLACC) Behavioural Scale by two trained, blinded, and independent study personnel. Both study personnel will measure pain at admission and discharge during the recovery phase.
Time Frame
Measure at patient admission and discharge at 30 minute intervals.
Title
Post-operative Pain
Description
Pain scores will be measured through a reliable and validated observer-rated Children's Hospital of Eastern Ontario Pain Scale (CHEOPS) by two trained, blinded, and independent study personnel. Both study personnel will measure pain at admission and discharge during the recovery phase.
Time Frame
Measure at patient admission and discharge at 30 minute intervals.

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
48 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males 6-48 months of age at presentation to Pediatric Urology clinics Patient who requires hypospadias repair by fellowship-trained Pediatric Urologists. Exclusion Criteria: Patients who have undergone previous hypospadias surgery Patients who have contraindications to either caudal or dorsal penile block Inability of parent/guardian to understand English/French Deviation to pre-established anesthesia protocol
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Luis Braga, MD
Phone
905-521-2100
Ext
73777
Email
braga@mcmaster.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Melissa McGrath
Phone
905-521-2100
Ext
73654
Email
mcgram2@mcmaster.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luis Braga, MD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
McMaster Children's Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 3Z5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luis Braga, MD
Phone
905-521-2100
Ext
73777
Email
braga@mcmaster.ca
Facility Name
Children's Hospital, London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sumit Dave
Phone
519-685-8439
Email
sumit.dave@lhsc.on.ca
Facility Name
Children's Hospital of Eastern Ontario
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L1
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luis Guerra, MD
Phone
613-737-7600
Ext
1353
Email
lguerra@cheo.on.ca
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Armando Lorenzo, MD
Phone
416-813-1500
Ext
203109
Email
armando.lorenzo@sickkids.ca

12. IPD Sharing Statement

Links:
URL
https://surgery.mcmaster.ca/divisions/pediatric-surgery/research/mpsrc
Description
McMaster Pediatric Surgery Research Collaborative

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Caudal vs Local Anesthesia in Hypospadias

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