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Leukemia-Lymphoma clinical trials

View clinical trials related to Leukemia-Lymphoma.

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NCT ID: NCT04003012 Completed - Leukemia-Lymphoma Clinical Trials

Pain Control in Pediatric Oncology: Utility of EMLA Cream vs Lidocaine Injection in Lumbar Punctures

Start date: July 19, 2019
Phase: Phase 4
Study type: Interventional

A common procedure in children with cancer is the spinal tap, or lumbar puncture (LP), in which a needle is inserted into the spinal canal. In this population, LPs are most commonly performed to collect cerebrospinal fluid (CSF, the liquid surrounding the brain and spinal cord) for diagnostic testing, and to inject medications including chemotherapy. Local analgesic (pain control medicine) during pediatric LP procedures is underutilized and not standardized. The first local analgesic routinely used for LP procedures was lidocaine injection. The discovery of the topical EMLA (lidocaine 2.5%/prilocaine 2.5%) cream, approved by the FDA for local skin use in pediatric patients, has provided an additional option for local LP analgesia. A comparison between topical EMLA vs lidocaine injection for LP pain control in the pediatric population has not been performed. Pediatric oncology patients often require serial LPs for diagnostics purposes and/or chemotherapy delivery. Due to a lack of standardization of LP analgesia in this population, the investigators have designed a prospective, single-blind, randomized control crossover trial to examine EMLA vs. lidocaine injection in reducing pain associated with LP in children being treated for leukemia or lymphoma.

NCT ID: NCT03413644 Completed - Leukemia-Lymphoma Clinical Trials

Evaluation of ClearLLab Leukemia and Lymphoma Panels

Start date: November 14, 2017
Phase:
Study type: Observational

Multi-center study of specimens from subjects presenting to the flow cytometry laboratory as part of their standard of care for hematological diseases work-up.

NCT ID: NCT01464047 Completed - Clinical trials for Leukemia, Myelomonocytic, Chronic

Korean Post-marketing Surveillance for Sprycel®

Start date: October 2011
Phase: N/A
Study type: Observational

The purpose of this post-marketing surveillance is to investigate and confirm the type and incidence of newly identified adverse events and any other factors affecting safety and efficacy of Sprycel® so that the regulatory authority can manage the marketing approval properly.