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Cryptorchidism clinical trials

View clinical trials related to Cryptorchidism.

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NCT ID: NCT01896076 Completed - Inguinal Hernia Clinical Trials

The Caudal Space in Children: Ultrasound Evaluation

Start date: June 2013
Phase: N/A
Study type: Observational

Caudal anesthesia is commonly employed in pediatrics to produce postoperative analgesia in low abdominal or urologic surgery. An exact understanding of the anatomy of the sacral area including sacral hiatus and surrounding structures is crucial to the success of caudal block. The aim of this study is to evaluate the anatomy of the caudal space in pediatrics by ultrasound evaluation.

NCT ID: NCT01701778 Completed - Inguinal Hernia Clinical Trials

Caudal Versus Intravenous Dexmedetomidine for Supplementation of Caudal Analgesia in Children

Start date: October 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effects of caudal dexmedetomidine with intravenous dexmedetomidine on caudal levobupivacaine analgesia in children undergoing lower abdominal surgeries.

NCT ID: NCT01604915 Completed - Cryptorchidism Clinical Trials

Comparison of Dexamethasone Added to Ropivacaine and Ropivacaine Alone in Caudal Analgesia in Children Undergoing Orchiopexy

Start date: May 2012
Phase: N/A
Study type: Interventional

Single shot caudal epidural block is one of the most widespread technique for pediatric pain management after infraumbilical surgical procedures. However, in a significant proportion of patients, despite good initial analgesia from a caudal block with local anesthetic, pain develops after the block resolves. In order to decrease postoperative analgesic requirements after caudal block, various drugs such as opioids, ketamine, clonidine, or dexmedetomidine to local anesthetics has been investigated. However, their use has been limited by adverse effects in children. Recently, many study suggested that epidurally administered dexamethasone could reduce the incidence and severity of postoperative pain in adults. But there is no study concerning the use of dexamethasone, as an adjuvant agent for the caudal epidural block in children. The investigators performed prospective randomized double-blind study to examine the analgesic effect of dexamethasone added to ropivacaine and ropivacaine alone in caudal analgesia on postoperative pain control in pediatric patients undergoing orchiopexy. 80 children (aged 0.5-5 yr) undergoing day-case orchiopexy were included in this prospective, randomized, double-blinded study. After inhalation induction of general anesthesia, caudal block was applied. Patients were randomly assigned in two groups. Normal saline 0.02mL/Kg added to ropivacaine 0.15% 1.5ml/kg was administered to Group R , dexamethasone 0.1mg/kg added to ropivacaine 0.15% 1.5ml/kg to Group DR. Postoperative pain was recorded at 30min and 1,2,3 h by using Hospital of Eastern Ontario Pain Scale (CHEOPS, 0-10) and Faces Legs Activity Cry Consolability tool (FLACC, 0-10). Participants will be followed for the duration of hospital stay, an expected average of 3 hours. After discharge, rescue analgesic consumption, pain scores, and adverse effects were evaluated for 24h. The time to first supplemental oral analgesic medication demand was defined as the time from the end of surgery to the first registration of a VAS ( 0-10) ≥ 5 by parent's observation. Twenty-four hours after surgery, reports of delayed side effects and demands for rescue analgesics from the child were gathered from parents via a telephone interview.

NCT ID: NCT00565513 Completed - Cryptorchidism Clinical Trials

Cryptorchidism: Impact of in Utero Exposure to Xenobiotics With Hormonal Action

Start date: April 2002
Phase: N/A
Study type: Interventional

We studied prospectively the incidence of cryptorchidism in Nice area. We tightly matched each affected child (n=95) with 2 healthy controls (n=188) and assessed risk factors for cryptorchidism focussing on prenatal exposure (cord blood and maternal milk) to endocrine disruptors known to affect testis migration, searching for correlations with cryptorchid status

NCT ID: NCT00435383 Completed - Cryptorchidism Clinical Trials

Comparing Oxygen Saturation in Post Anesthesia Care Unit After Different Methods of Pain Relief

Start date: March 2003
Phase: Phase 2
Study type: Observational

To determine the which method of pain relief is better after current anesthesia care.

NCT ID: NCT00264121 Recruiting - Undescended Testis Clinical Trials

The Incidence of Congenital Undescended Testis Among Dutch Infants

Start date: June 2005
Phase: N/A
Study type: Observational

The purpose of this study is to determine the incidence of congenital undescended testis of mature boys, at one year of age, born in the Medical Centre Alkmaar (MCA).

NCT ID: NCT00253253 Completed - Undescended Testis Clinical Trials

Long-Term Outcome in Congenital Undescended Testis After Surgical Treatment by Orchidopexy

Start date: August 2006
Phase: N/A
Study type: Observational

The purpose of this study is to determine the long-term outcome in congenital undescended testis after surgical treatment by orchidopexy and to what extent orchidopexy is the treatment for congenital undescended testis.