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Antibiotic Use in Distal Hypospadias Repair

Primary Purpose

Hypospadias

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Randomization to not receive prophylactic antibiotics after surgery.
Randomization to receive prophylactic antibiotics after surgery
Sponsored by
Arkansas Children's Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypospadias focused on measuring distal hypospadias repair, urinary tract infection, prophylactic antibiotic use

Eligibility Criteria

3 Months - 6 Years (Child)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Males undergoing primary distal hypospadias repair with open urethral stent drainage.

Exclusion Criteria:

  • Males undergoing fistula repair or glandular hypospadias repair without incontinent urethral stent drainage and hypospadias repair of mid or more proximal degrees of hypospadias were excluded from this study.

Sites / Locations

  • Arkansas Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Antibiotics prophylaxis cohort

Antibiotic-sparing cohort

Arm Description

Subjects were prescribed prophylactic antibiotics after the hypospadias surgery.

Subjects were not prescribed prophylactic antibiotics after the hypospadias surgery.

Outcomes

Primary Outcome Measures

Prevalence of symptomatic UTI within 30 days post-surgery
Assess the prevalence of symptomatic UTI in subjects receiving standard of care dispensation of prophylaxis versus subjects selected to an antibiotic-sparing cohort.

Secondary Outcome Measures

Evaluation of surgical site infections (SSIs) and complications of hypospadias repair
Surgical site infections (SSIs) are measured using physical assessments at the stent removal visit. Complications of hypospadias repair (urethral fistula, meatal stenosis, dehiscence, and diverticulum) are measured using physical assessments at the stent removal visit and/or contact with the family or the PCP office 1 week after the stent removal; at the 30 day post operative time point; and at the 3 month follow-op visit.

Full Information

First Posted
August 11, 2017
Last Updated
September 6, 2017
Sponsor
Arkansas Children's Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03275519
Brief Title
Antibiotic Use in Distal Hypospadias Repair
Official Title
Randomized Trial of Antibiotic Prophylaxis for Prevention of Symptomatic UTI in Stented, Distal Hypospadias Repair
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
January 19, 2015 (Actual)
Primary Completion Date
February 17, 2017 (Actual)
Study Completion Date
April 19, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Arkansas Children's Hospital Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypospadias is a common condition where the opening of the penis is not located at the tip, but along the underside of the penis. It is estimated to occur in 1/300 live male births, making it one of the most common birth defects. Degrees of hypospadias ranged from minor to severe depending on the location of the opening. Surgical repair is often required and involves placement of a catheter for the urine to drain with known urinary colonization found on prior retrospective studies. The current practice of using preventative antibiotics as long as the catheter is in place is conflicting with resent studies that show antibiotics may not be necessary to prevent urinary tract infections (UTIs). The purpose of this study was to see how common symptomatic UTIs were after hypospadias repair surgery; and to see whether routine antibiotic use after surgery affected the rate of UTIs. Subjects were randomized to either receive antibiotics or no antibiotics after distal hypospadias repair. The research coordinator made follow-up phone calls with the family and the primary care provider (PCP) after stent removal, 30 days post surgery and after the 3 month post surgical visit.
Detailed Description
Males undergoing distal hypospadias repair involving stent placement were randomized to either receive or not to receive antibiotics post-operative. All subjects did not receive intra-operative antibiotics. Routine follow-up included having the stent removed one week post-op and a return visit at 3 months. The research nurse made follow-up phone calls to the family or the (PCP) one week after the stent was removed and at one month post-op to see how things were going with the child and again after teh 3 month post surgical visit, if the subject did not return after multiple rescheduling attempts.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypospadias
Keywords
distal hypospadias repair, urinary tract infection, prophylactic antibiotic use

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Using the block randomization procedures, a subject was assigned to a study group by computer using the REDCap randomization module. Subjects were randomized to receive post operative antibiotics or to not receive any antibiotics postoperative.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Antibiotics prophylaxis cohort
Arm Type
Active Comparator
Arm Description
Subjects were prescribed prophylactic antibiotics after the hypospadias surgery.
Arm Title
Antibiotic-sparing cohort
Arm Type
Active Comparator
Arm Description
Subjects were not prescribed prophylactic antibiotics after the hypospadias surgery.
Intervention Type
Other
Intervention Name(s)
Randomization to not receive prophylactic antibiotics after surgery.
Intervention Description
No antibiotics were ordered after surgery.
Intervention Type
Other
Intervention Name(s)
Randomization to receive prophylactic antibiotics after surgery
Intervention Description
In general, the antibiotic given is a combination sulfamethoxazole/ trimethoprim oral suspension (2-3 mg trimethoprim/kg by mouth once a day); or if indicated, nitrofurantoin (1mg/kg by mouth once daily). All subjects did not receive intraoperative antibiotics.
Primary Outcome Measure Information:
Title
Prevalence of symptomatic UTI within 30 days post-surgery
Description
Assess the prevalence of symptomatic UTI in subjects receiving standard of care dispensation of prophylaxis versus subjects selected to an antibiotic-sparing cohort.
Time Frame
30 days post surgery
Secondary Outcome Measure Information:
Title
Evaluation of surgical site infections (SSIs) and complications of hypospadias repair
Description
Surgical site infections (SSIs) are measured using physical assessments at the stent removal visit. Complications of hypospadias repair (urethral fistula, meatal stenosis, dehiscence, and diverticulum) are measured using physical assessments at the stent removal visit and/or contact with the family or the PCP office 1 week after the stent removal; at the 30 day post operative time point; and at the 3 month follow-op visit.
Time Frame
Approximately post surgery: 2 weeks (stent is in approximately 1 week and then 1 week after the stent is removed); 30 days; and 3 months

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Males undergoing hypospadias repair on their penis.
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Males undergoing primary distal hypospadias repair with open urethral stent drainage. Exclusion Criteria: Males undergoing fistula repair or glandular hypospadias repair without incontinent urethral stent drainage and hypospadias repair of mid or more proximal degrees of hypospadias were excluded from this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen Canon
Organizational Affiliation
Arkansas Children's Hospital, Pediatric Urology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Arkansas Children's Hospital
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72202
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Antibiotic Use in Distal Hypospadias Repair

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