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2-octyl Cyanoacrylate for Closure of Urethrocutaneous Fistula.

Primary Purpose

Urethrocutaneous Fistulas

Status
Completed
Phase
Phase 3
Locations
Mexico
Study Type
Interventional
Intervention
2-octylcyanoacrylate
Surgical reintervention
Sponsored by
Instituto Mexicano del Seguro Social
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urethrocutaneous Fistulas focused on measuring 2-octylcyanoacrylate, Urethrocutaneous fistulas., Closure., Recurrence.

Eligibility Criteria

6 Months - 5 Years (Child)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Children younger than 5 years old with at least one postoperative UCF with an external orifice less than 5 mm in diameter at the distal, proximal or medial penis,
  • Patients whose parents or guardians accepted inclusion in the study by signing the informed consent form

Exclusion Criteria:

  • Patients with an external orifice more than 5 mm in diameter
  • Iatrogenic or traumatic fistulae
  • The presence of obstruction distal to the fistula, necrotic tissue or active infection at the surgical site,
  • The presence of chronic diseases such as diabetes mellitus, renal or hepatic insufficiency, malignancy of any type or use of steroids and/or immunosuppressive therapy of any kind,

Sites / Locations

  • Department of Pediatric Surgery of the Pediatrics Hospital of the Western Medical Center of the Mexican Institute of Social Security

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

2-octylcyanoacrylate

Surgical reintervention

Arm Description

Application of 2-octylcyanoacrylate

Surgical reintervention for urethrocutaneous fistula repair

Outcomes

Primary Outcome Measures

Use of 2-octylcyanoacrylate for closure urethrocutaneous fistulas after urethroplasty for hypospadias.
Closure or recurrence of urethrocutaneous fistulas after cyanoacrylate application or surgical intervention.

Secondary Outcome Measures

Morbidity after applications
Morbidity after applications of cyanoacrylates or surgical reintervention.

Full Information

First Posted
April 13, 2014
Last Updated
September 29, 2023
Sponsor
Instituto Mexicano del Seguro Social
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1. Study Identification

Unique Protocol Identification Number
NCT02115191
Brief Title
2-octyl Cyanoacrylate for Closure of Urethrocutaneous Fistula.
Official Title
Use of 2-octylcyanoacrylate for Closure Urethrocutaneous Fistulas After Urethroplasty for Hypospadias
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
January 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Mexicano del Seguro Social

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Urethrocutaneous fistulae (UCF) represent one of the most frequent causes of morbidity after urethroplasty. Hypospadias can be repaired using different surgical techniques, but regardless of technique, the incidence of UCF ranges between 10% and 40%. The surgical repair of UCF remains the treatment of choice, even if some patients need further operations because of recurrences. The cyanoacrylates have been used as skin suture substitutes, and some evidence suggests a beneficial effect when these adhesives are used as an adjuvant in the management of UCF.
Detailed Description
Design Randomized clinical trial carried out in children with UCF that occurred after hypospadias repair. The patients will be assign to either the control or study groups. The study group will include children with long-standing UCF that occurred at least 6 months after the initial intervention. After preparation of the fistula area, multiple layers of OCA will be apply, attaching the edges of the orifice. The same procedure will be repeated three times and the children will be follow for at least 6 months after treatment. The control group will include children with long-standing UCF that occurred at least 6 months after the initial intervention. Patients will be scheduled for surgical treatment and will be follow for at least 6 months after surgery. If UCF recurred, a new intervention will be proposed. The sample size was determined based on a prevalence of the complication (UCF) of 25% in the surgery group and 70% in the medically treated group, given a confidence level of 95% and a power of 0.20, which resulted in a minimum sample size of 18 patients per group. The independent variables are the application of OCA in the UCF orifice or surgical treatment of UCF and the main outcome variable is FC without recurrence within at least 12 months follow-up. As confounding variables, we considered the children's age, the fistulous orifice diameter and the type of initial surgical procedure to which all were submitted. Procedure Assignment of patients to groups will be performed by using a sealed envelope chosen randomly by the father, mother or guardians. To decrease the inflammatory response and edema, patients in the study group will be instructed to apply triamcinolone cream to the fistula four times a day for 3 days. Once this treatment is completed, the patient will attended our clinic as an outpatient to undergo, after sedation with midazolam (0.5 mg/kg orally), Foley catheterization with a 10 Fr gauge siliconized catheter, with the balloon inflated with 1.5 ml water to prevent bladder spasm. Subsequently, we will apply an adhesive using dissecting forceps to approximate the edges of the UCF, and then applied several thin layers of OCA. The urethral catheter will be left in place for 5 days. At the end of this time, we will evaluate the closure or persistence of the UCF. If the UCF persist, the OCA adhesive will be apply twice following the same protocol before the medical procedure was deemed to have failed. Patients in the control group will wait 6 months to be treated surgically. The reoperation consist on mobilizing dartos flaps and closing the defect in layers with absorbable sutures. Urinary bladder drainage will be provide with a 10 Fr silicone Foley catheter, with the balloon inflated with 1.5 ml water to prevent bladder spasm. The follow-up time will be 12 months for each group. Statistical analysis Statistical analysis Statistical software, SPSS for IBM (version 20 for Windows; IBM Corp., Armonk, NY, USA) is being used for data analysis. The data obtained will be expressed as frequencies and percentages, means and standard deviations. For comparing results, Student's t test will be used for continuous variables and Chi2 or Fisher's exact tests will be used for qualitative data when appropriate. Relative risk (RR) and 95% confidence intervals (95% CI) will be determined as well as the absolute risk reduction (ARR), relative risk reduction (RRR), and number needed to treat (NNT). Statistical significance from two-tailed tests was assumed when p < 0.05

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urethrocutaneous Fistulas
Keywords
2-octylcyanoacrylate, Urethrocutaneous fistulas., Closure., Recurrence.

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
2-octylcyanoacrylate
Arm Type
Experimental
Arm Description
Application of 2-octylcyanoacrylate
Arm Title
Surgical reintervention
Arm Type
Active Comparator
Arm Description
Surgical reintervention for urethrocutaneous fistula repair
Intervention Type
Device
Intervention Name(s)
2-octylcyanoacrylate
Intervention Description
After sedation with midazolam (0.5 mg/kg orally) a Foley catheterization with a 10 Fr gauge siliconized catheter will be placed, with the balloon inflated with 1.5 ml water to prevent bladder spasm. After this we will apply the adhesive by using dissecting forceps to approximate the edges of the UCF, and then apply it several thin layers of OCA.
Intervention Type
Procedure
Intervention Name(s)
Surgical reintervention
Intervention Description
The reoperation will consist on mobilizing dartos flaps and closing the defect in layers with absorbable sutures. Urinary bladder drainage will be provided with a 10 Fr silicone Foley catheter, with the balloon inflated with 1.5 ml water to prevent bladder spasm.
Primary Outcome Measure Information:
Title
Use of 2-octylcyanoacrylate for closure urethrocutaneous fistulas after urethroplasty for hypospadias.
Description
Closure or recurrence of urethrocutaneous fistulas after cyanoacrylate application or surgical intervention.
Time Frame
12 months after procedure.
Secondary Outcome Measure Information:
Title
Morbidity after applications
Description
Morbidity after applications of cyanoacrylates or surgical reintervention.
Time Frame
12 months after the procedure.

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children younger than 5 years old with at least one postoperative UCF with an external orifice less than 5 mm in diameter at the distal, proximal or medial penis, Patients whose parents or guardians accepted inclusion in the study by signing the informed consent form Exclusion Criteria: Patients with an external orifice more than 5 mm in diameter Iatrogenic or traumatic fistulae The presence of obstruction distal to the fistula, necrotic tissue or active infection at the surgical site, The presence of chronic diseases such as diabetes mellitus, renal or hepatic insufficiency, malignancy of any type or use of steroids and/or immunosuppressive therapy of any kind,
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alejandro González-Ojeda, Ph.D., M.D.
Organizational Affiliation
Instituto Mexicano del Seguro Social
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Pediatric Surgery of the Pediatrics Hospital of the Western Medical Center of the Mexican Institute of Social Security
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44340
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
25416602
Citation
Ambriz-Gonzalez G, Aguirre-Ramirez P, Garcia-de Leon JM, Leon-Frutos FJ, Montero-Cruz SA, Trujillo X, Fuentes-Orozco C, Macias-Amezcua MD, del Socorro Alvarez-Villasenor A, Cortes-Flores AO, Chavez-Tostado M, Gonzalez-Ojeda A. 2-octyl cyanoacrylate versus reintervention for closure of urethrocutaneous fistulae after urethroplasty for hypospadias: a randomized controlled trial. BMC Urol. 2014 Nov 21;14:93. doi: 10.1186/1471-2490-14-93.
Results Reference
derived

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2-octyl Cyanoacrylate for Closure of Urethrocutaneous Fistula.

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