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Incidence of Urethrocutaneous Fistula With and Without Caudal Epidural Block

Primary Purpose

Distal Hypospadias

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Ropivacaine
Fentanyl Citrate
Sponsored by
Sir Ganga Ram Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Distal Hypospadias

Eligibility Criteria

1 Year - 8 Years (Child)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male children l
  2. 1 to 8 years of age
  3. ASA physical status I and II
  4. Distal hypospadias -

Exclusion Criteria:

  1. Simultaneously undergoing any other procedure
  2. Local infection in sacral region
  3. Bleeding diathesis
  4. Preoperative testosterone stimulation

Sites / Locations

  • Sir Ganga Ram Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Caudal Group

Non- Caudal Group

Arm Description

Children will receive oral midazolam 0.25 mg/kg thirty minutes before induction. Inhalational induction will be carried with incremental concentration of sevoflurane upto 8% in 50% oxygen and nitrous oxide mixture. As soon as the child will be asleep, ASA standard monitors (SPO2, HR, ECG and NIBP) will be attached. Intravenous access with age appropriate IV cannula will be secured. Injection fentanyl citrate 2 mcg/ kg followed by injection atracurium 0.5 mg/kg will be administered. Appropriate size LMA Pro SealTM will be inserted and pressure controlled ventilation will be instituted. Children in will then receive CEB with 0.2 % ropivacaine 1-ml/kg for maintaining analgesia

Children will receive oral midazolam 0.25 mg/kg thirty minutes before induction. Inhalational induction will be carried with incremental concentration of sevoflurane upto 8% in 50% oxygen and nitrous oxide mixture. As soon as the child will be asleep, ASA standard monitors (SPO2, HR, ECG and NIBP) will be attached. Intravenous access with age appropriate IV cannula will be secured. Injection fentanyl citrate 2-mcg/ kg followed by injection atracurium 0.5 mg/kg will be administered. Appropriate size LMA Pro SealTM will be inserted and pressure controlled ventilation will be instituted. Children in will then receive fentanyl citrate 1-mcg/kg/hr for maintaining analgesia

Outcomes

Primary Outcome Measures

Incidence of urethrocutaneous fistula
Patients undergoing distal hypospadias repair will be followed up for occurrence of uretherocutaneous fistula

Secondary Outcome Measures

Penile Engorgement
Length of penis from pubic bone to glans tip and mid shaft circumference i.e. girth around the widest part of the penile shaft will be calculated
Changes in intra-operative heart rate (beats per minute)
Comparison of intra-operative heart rate between both the arms will be done
Change in Intra-operative blood pressure - systolic , diastolic, and mean (mmHg)
Comparison of intra-operative blood pressure- systolic, diastolic, and mean between both the arms will be done
Postoperative analgesia requirement
Additional fentanyl citrate 0.5-mcg/kg will be administered intravenously if the Face, Legs, Activity, Cry, Consolability scale (FLACC scale) score is > 3 and total amount administered will be recorded
Incidence of complications
Complications of surgery such as infection, bleeding , hematoma, glans dehiscence, skin or flap necrosis will be noted

Full Information

First Posted
January 19, 2019
Last Updated
October 29, 2020
Sponsor
Sir Ganga Ram Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03812731
Brief Title
Incidence of Urethrocutaneous Fistula With and Without Caudal Epidural Block
Official Title
Incidence of Urethrocutaneous Fistula Following Distal Hypospadias Repair With and Without Caudal Epidural Block - A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
February 22, 2019 (Actual)
Primary Completion Date
November 28, 2019 (Actual)
Study Completion Date
November 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sir Ganga Ram Hospital

4. Oversight

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

5. Study Description

Brief Summary
The study is designed to explore any association between the caudal epidural block(CEB) given for perioperative analgesia and the occurrence of urethrocutaneous fistula postoperatively in children undergoing distal hypospadias repair .We also intend to study the duration of penile engorgement due to CEB causing penile oedema which may subsequently play a role in fistula formation. The pilot study will recruit children under 8 years of age diagnosed with distal hypospadias scheduled to undergo Tubularised Incised Plate Urethroplasty, operated by a single paediatric surgeon. General anaesthesia will be induced with sevoflurane in oxygen nitrous oxide mixture supplemented by fentanyl citrate and atracurium besylate in all children. LMA Pro SealTMof appropriate size will be inserted. Children in group I will then be given caudal epidural block (CEB) as per our practice protocol. Children in group II will be given additional intravenous fentanyl citrate. All children will be followed postoperatively till 3 months to evaluate incidence of urethtocutaneous fistula. The prospective study attempts to eliminate previously reported confounding factors.
Detailed Description
CEB is routinely used along with general anaesthesia for inguinal and genital surgeries. It provides intraoperative and postoperative analgesia, is safe, simple and has success rate of more than 90% in children.It decreases the requirement of inhalational anaesthetics and narcotics, decreases stress hormone release and facilitates early recovery. Hypospadias is the most common congenital anomaly of penis, incidence being 1 in 300 live births. Hypospadias repair is a technical procedure that can be associated with significant complications such as meatal stenosis, stricture, glans dehiscence and flap necrosis Urethrocutaneous fisula formation is the most common complication after primary repair with an incidence of upto 20%. There have been controversies regarding the association of CEB with urethrocutaneous fistula. Some studies have reported a high incidence of postoperative urethrocutaneous fistula in children who received CEB while others have not confirmed any such relationship. Association between urethrocutaneous fistula and site of urethral opening, age of patient, duration of surgery, surgeon's expertise, use of subcutaneous epinephrine and use of preoperative testosterone has been found. Penile engorgement, post inflammatory response and tissue oedema may be contributory factors for development of fistula. However any association between CEB and fistula formation is not clear. All studies, except one, are retrospective, limited by small sample size and presence of various confounding factors. The present study is aimed to explore any association between CEB and urethrocutaneous fistula. The study will be conducted in children with distal hypospadias only; they will be operated by a single surgeon, without the use of subcutaneous epinephrine, so that any association, if at all between CEB and urethrocutaneous fistula becomes evident.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Distal Hypospadias

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
30 male patients aged 1-8 years, ASA physical status I/II, and undergoing distal hypospadias repair will be randomly allocated to one of the following two groups: GROUP I- (Caudal group, n= 15) Children will receive general anesthesia (GA) and analgesia will be maintained with caudal epidural block (CEB) with 0.2% ropivacaine:1 ml/kg. GROUP II- (Non-caudal group, n= 15) Children will receive general anaesthesia (GA) and analgesia will be maintained with intravenous fentanyl citrate 1mcg/kg/hr. roup-1 [CLADS Group, n=60]: Anaesthesia will be induced and maintained with propofol administered using the BIS feedback-based automated CLADS. Group-2 [Desflurane Group, n=60]: Anaesthesia will be induced with propofol CLADS and will be maintained intraoperatively by Desflurane titrated to BIS monitoring.
Masking
ParticipantOutcomes Assessor
Masking Description
The attending anaesthesiologist will not be blinded to the technique utilised to administer GA. An independent assessor blinded to the technique of GA will follow up the patients to determine the incidence of uretherocutaneous fistula
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Caudal Group
Arm Type
Active Comparator
Arm Description
Children will receive oral midazolam 0.25 mg/kg thirty minutes before induction. Inhalational induction will be carried with incremental concentration of sevoflurane upto 8% in 50% oxygen and nitrous oxide mixture. As soon as the child will be asleep, ASA standard monitors (SPO2, HR, ECG and NIBP) will be attached. Intravenous access with age appropriate IV cannula will be secured. Injection fentanyl citrate 2 mcg/ kg followed by injection atracurium 0.5 mg/kg will be administered. Appropriate size LMA Pro SealTM will be inserted and pressure controlled ventilation will be instituted. Children in will then receive CEB with 0.2 % ropivacaine 1-ml/kg for maintaining analgesia
Arm Title
Non- Caudal Group
Arm Type
Active Comparator
Arm Description
Children will receive oral midazolam 0.25 mg/kg thirty minutes before induction. Inhalational induction will be carried with incremental concentration of sevoflurane upto 8% in 50% oxygen and nitrous oxide mixture. As soon as the child will be asleep, ASA standard monitors (SPO2, HR, ECG and NIBP) will be attached. Intravenous access with age appropriate IV cannula will be secured. Injection fentanyl citrate 2-mcg/ kg followed by injection atracurium 0.5 mg/kg will be administered. Appropriate size LMA Pro SealTM will be inserted and pressure controlled ventilation will be instituted. Children in will then receive fentanyl citrate 1-mcg/kg/hr for maintaining analgesia
Intervention Type
Drug
Intervention Name(s)
Ropivacaine
Intervention Description
Intraoperatively after induction of anaesthesia caudal epidural block will be administered with 0.2% ropivacaine 1-ml/kg
Intervention Type
Drug
Intervention Name(s)
Fentanyl Citrate
Intervention Description
Intraoperatively after induction of anaesthesia fentanyl 1-mcg/kg/hour will be administered
Primary Outcome Measure Information:
Title
Incidence of urethrocutaneous fistula
Description
Patients undergoing distal hypospadias repair will be followed up for occurrence of uretherocutaneous fistula
Time Frame
From one day after surgery(0-hours, baseline) till 3-months post surgery
Secondary Outcome Measure Information:
Title
Penile Engorgement
Description
Length of penis from pubic bone to glans tip and mid shaft circumference i.e. girth around the widest part of the penile shaft will be calculated
Time Frame
After induction of anaesthesia (0-hours, baseline) till end of surgery
Title
Changes in intra-operative heart rate (beats per minute)
Description
Comparison of intra-operative heart rate between both the arms will be done
Time Frame
From beginning of anesthesia (0-hours, baseline) till 2-hours intraoperatively
Title
Change in Intra-operative blood pressure - systolic , diastolic, and mean (mmHg)
Description
Comparison of intra-operative blood pressure- systolic, diastolic, and mean between both the arms will be done
Time Frame
rom beginning of anesthesia (0-hours, baseline) till 2-hours intraoperatively
Title
Postoperative analgesia requirement
Description
Additional fentanyl citrate 0.5-mcg/kg will be administered intravenously if the Face, Legs, Activity, Cry, Consolability scale (FLACC scale) score is > 3 and total amount administered will be recorded
Time Frame
From end of anaesthesia (0-hours, baseline) till 24-hours postoperatively
Title
Incidence of complications
Description
Complications of surgery such as infection, bleeding , hematoma, glans dehiscence, skin or flap necrosis will be noted
Time Frame
From end of anaesthesia (0-hours, baseline) till 3-months postoperatively

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Only male patients with distal hypospadias will be included
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male children l 1 to 8 years of age ASA physical status I and II Distal hypospadias - Exclusion Criteria: Simultaneously undergoing any other procedure Local infection in sacral region Bleeding diathesis Preoperative testosterone stimulation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deepali Shukla, DA
Organizational Affiliation
Sir Ganga Ram Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Archna Koul, MS, MCH
Organizational Affiliation
Sir Ganga Ram Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Sir Ganga Ram Hospital
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110060
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No

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Incidence of Urethrocutaneous Fistula With and Without Caudal Epidural Block

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