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Hypospadias clinical trials

View clinical trials related to Hypospadias.

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NCT ID: NCT03275519 Completed - Hypospadias Clinical Trials

Antibiotic Use in Distal Hypospadias Repair

Start date: January 19, 2015
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT03145415 Completed - Clinical trials for Hypospadias and Epispadias

Comparison of Pudendal Nerve Block and Caudal Block for Hypospadias in Young Children

Start date: February 17, 2017
Phase: N/A
Study type: Interventional

The purpose of this randomized blinded prospective study is to compare the analgesic efficacy and duration of a Pudendal Nerve Block (PNB) to a Caudal Block (CB) for pediatric patients, ages 6 months to 2 years, undergoing hypospadias repair.

NCT ID: NCT03102554 Active, not recruiting - Hypospadias Clinical Trials

Genetics of Differences of Sex Development and Hypospadias

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

This study seeks to identify genetic causes of conditions that affect the gonads and genitals, and to study the impact on families of receiving genetic results.

NCT ID: NCT02861950 Active, not recruiting - Hypospadias Clinical Trials

Does Caudal Block Increase the Incidence of Urethrocutaneous Fistula Formation Following Hypospadias Repair in Infants?

Start date: May 24, 2017
Phase: Phase 4
Study type: Interventional

This is a prospective randomized multi-center non-inferiority trial conducted through the Pediatric Regional Anesthesia Network study sites to determine if caudal block increases the incidence of urethrocutaneous fistula following distal or mid shaft hypospadias repair compared with penile nerve block.

NCT ID: NCT02851290 Completed - Hypospadias Clinical Trials

Effect of Caudal and Penile Block on Hypospadias Repair Complications

Start date: July 2016
Phase: N/A
Study type: Interventional

Hypospadias is one of the most common genitourinary (GU) malformations, seen in approximately 1 of 250 male live births. Common methods of local anesthesia administration for hypospadias surgery include caudal and dorsal penile nerve blocks. While both methods are known to be effective with minimal risk, the effect on post-operative complications is not well-established. The purpose of this randomized controlled trial is to evaluate if caudal versus dorsal penile nerve block results in higher rates of post-operative complications.

NCT ID: NCT02848157 Completed - Hypospadias Clinical Trials

Effects of Dexmedetomidine as Adjunct to Pudendal Block for Pediatric Penile Surgery

Start date: June 17, 2016
Phase: Phase 4
Study type: Interventional

Caudal block is often performed to relieve postoperative pain in pediatric urological surgery. Recently, pudendal block is also used in penile surgery and it has advantage because of less side effects such as transient weakness of low extremities, but limited to use in penile surgery. Local anesthesia is a single shot injection, so additional analgesic drugs is required when the effect of local anesthetics are disappeared. Dexmedetomidine, an alpha adrenergic agonist, is commonly used in pediatric sedation. It has analgesic effect and potentiates the effect of local anesthetics. There are many studies about the potentiation of the effect of local anesthetics when added to dexmedetomidine in adults, it has been limited in pediatrics. Recent study said that local anesthetics with dexmedetomidine had prolonged duration of analgesia in caudal block, also in ilioinguinal block. Thus it is expected to have a prolonged effect when investigators use dexmedetomidine in pediatrics as well as adults.

NCT ID: NCT02805491 Completed - Hypospadias Clinical Trials

Influence of Pesticide Exposure on the Occurrence of Hypospadias in Newborns in Picardie

HYPOMECO
Start date: March 3, 2011
Phase:
Study type: Observational

We want to see if there is a relationship between exposure to pesticides and the occurrence of hypospade in Picard newborn .

NCT ID: NCT02769390 Completed - Postoperative Pain Clinical Trials

Association of Different Doses of Clonidine in Caudal Epidural Anesthesia for Hypospadias Surgery

clonidine
Start date: July 2015
Phase: Phase 2
Study type: Interventional

The use of increasing doses of clonidine ssociated to bupivacaine in caudal epidural block provides better postoperative analgesia compared whit analgesia provide by bupivacaine alone It is a randomized, double blind study, involving 80 children with ages from 1 to 10 years old, following eletive hypospadias surgery, under general anesthesia and caudal epidural block . The patients will be divided into 4 groups: bupivacaine alone, bupivacaine plus clonidine 1mcg/kg, bupivacaine plus clonidine 2 mcg/kg, bupivacaine plus clonidine 3 mg/kg. The peroperative consumption of anesthetics gases, heart rate and arterial blood pressure will be recorded. Postoperative pain will be evaluated by using FLACC scale ( faces , legs, activity , cry , consolability ) . Requiriments for supplementary postoperative analgesia at 24 h will be avaiable.

NCT ID: NCT02752308 Completed - Hypospadias Clinical Trials

Effectiveness of Caudal Epidural Block on Intraoperative Blood Loss During Hypospadias Repair

Start date: September 2014
Phase: Phase 2/Phase 3
Study type: Interventional

From September 2014 to March 2015, 57 consecutive patients with hypospadias who are candidate for surgery will be enrolled in this randomized clinical trial. Regional ethics committee of Isfahan University of Medical Sciences approved the protocol of the study and all parents will sign a written informed consent. Inclusion criteria are age between 6 months to 15 years and hypospadias with any severity. Exclusion criteria are coagulopathy, history of previous failed surgery, skin infection , parents' disagreement with the protocol and any cardiac problem that made epinephrine injection contraindicated. All selected patients will randomly allocate to one of the two groups: group A will receive caudal epidural block (CEB) plus general anesthesia before surgery and group B will receive general anesthesia before surgery and CEB afterwards. The surgical procedures will be performed by a single pediatric urologist (FA). The surgical technique will be tubularized incised plate in all cases. Intraoperative blood loss will be determined by weighing all surgical gauzes used during procedure with a digital scale measure to the nearest 0.01 gram, every 10 minutes to minimize the effect of water vaporization on gauzes weights. In addition to blood loss, operation time, dose of fentanyl used during procedure and length of the urethral plate defect will be recorded for each patient by trained nurses. Demographics and disease characteristics as well as operation details will be compared in the two studied groups.

NCT ID: NCT02593903 Completed - Hypospadias Clinical Trials

Antibiotic Use Following Distal and Mid-shaft Hypospadias Repair

Start date: March 4, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of prophylactic antibiotics following distal or mid-shaft hypospadias repair in influencing the rate of postoperative urinary tract infection and complications.