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Anesthesia, Caudal clinical trials

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NCT ID: NCT05581940 Completed - Pain, Postoperative Clinical Trials

Pediatric Caudal Anesthesia Block. And Pain Control

CEB
Start date: January 5, 2020
Phase:
Study type: Observational [Patient Registry]

Caudal epidural block CEB is the most commonly performed neuraxial block to provide effective pain relief and analgesia in patients undergoing infra-umbilical pediatric surgery. This study aimed to compare the effectiveness of adding CEB to general anesthesia in terms of intra- and post-operative pain management. Design: Double-unblinded. Prospective. randomized. Study, Setting: salmanyia medical complex. intraoperative, postoperative recovery room Methods: A total of 72 patients American Society of Anesthesiology physical status classification ASA 1. Patients were equally allocated into two groups Group A and with CEB and Group B without CEB, aged two months to six years. respectively, over a study period of six months. Both groups were compared based on hemodynamic stability, level of sedation, analgesia need, pain score, and parental satisfaction. Postoperative pain was evaluated by four different pain scales.

NCT ID: NCT05133687 Completed - Pediatrics Clinical Trials

The Hemodynamic Effects of Different Volumes of Bupivacaine 0.25% Caudal Blocks in Pediatrics Undergoing Lower Abdominal Surgeries as Measured by Electrical Cardiometry

Start date: November 1, 2021
Phase: Phase 3
Study type: Interventional

This randomized, controlled study is designed to estimate the effects of different volumes of plain bupivacaine 0.25% caudal block on different hemodynamic parameters assessed by electrical cardiometry.

NCT ID: NCT04590027 Completed - Anesthesia, Caudal Clinical Trials

Caudal Block Versus Local Wound Infiltration for Inguinal Procedures

Start date: February 1, 2014
Phase:
Study type: Observational

Single-centre observational study to analyse whether there is a difference in post-operative pain scores and set up time when comparing caudal block with local wound infiltration

NCT ID: NCT04491032 Completed - Pediatrics Clinical Trials

Pediatric Caudal Injection Volume on Optic Nerve Sheath Diameter and Cerebral Oxygenation

Start date: February 15, 2019
Phase: N/A
Study type: Interventional

Caudal anesthesia is a commonly used neuraxial anesthesia method for children. Injection of a certain volume of fluid into the epidural space for cauda anesthesia may push some cerebrospinal fluid towards the head, which may lead to mild increase of pressures inside the head. Such mild changes are compensated well by healthy individuals and no clinical sequel is seen, however at-risk populations may be affected. We aim to see how different amounts of fluid injected into the epidural space may change two clinical parameters affected by intracranial pressure to determine if a lower volume is safer than a higher one.

NCT ID: NCT03825172 Completed - Ultrasonography Clinical Trials

Evaluation Of Caudal Epidural Anatomy By Ultrasonography İn Pediatric Patients

Start date: January 28, 2019
Phase:
Study type: Observational [Patient Registry]

Detailed study of ultrasonographic caudal epidural anatomy

NCT ID: NCT02233309 Completed - Anesthesia, Caudal Clinical Trials

A Prospective Observational Study of Epidural Pressures During Caudal Epidural in the Pediatric Population

Start date: April 2014
Phase: N/A
Study type: Observational

This study is a prospective study of epidural pressure changes when local anesthetic is injected from the caudal route. All patients will receive the same weight based volume dose of local anesthetic after induction of general anesthesia, and a CVP transducer will be attached to the standard caudal needle for measurement of pressure: under the skin, after entering the epidural space, and every 15 seconds for 3 minutes after completion of injection with the needle in situ. The placement of the caudal epidural will follow current standard of care and administration, the only variation will be the addition of a pressure transducer to the stopcock where the local anesthetic syringe is attached that will allow for pressure monitoring.

NCT ID: NCT01869036 Completed - Anesthesia, Caudal Clinical Trials

Use of Caudal Anesthesia Supplemented With Morphine in Children Undergoing Renal Surgery

Start date: July 2012
Phase: Phase 4
Study type: Interventional

The aim of this study is to test an efficacy and safety of supplemented by Morphine caudal anesthesia in children who undergo renal surgery in our department.

NCT ID: NCT01107873 Completed - Anesthesia, Caudal Clinical Trials

Changes of Dorsalis Pedis Artery Flow Pattern After Caudal Block in Children: Observational Study Using a Duplex Sonography

Start date: May 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine the changes of Dorsalis Pedis Artery Flow Pattern after Caudal Block in Children: Observational Study Using a Duplex Sonography.