Accuvein clinical trials

Listing a study does not mean it has been evaluated by the U. Federal Government. Read our disclaimer for details. Last Update Posted : September 23, Study Description. The objective of this study is to evaluate the effectiveness of Accuvein to facilitate venous blood sampling and placement of peripheral intravenous catheters in adults.

This clinical protocol is designed to determine whether using Accuvein increases the ease and efficiency of venous cannulation as perceived by the operator , decreases the time to effective cannulation, decreases the number of sticks, and decreases the patient's perception of the pain.

Arms and Interventions. Accuvein will be used to facilitate venous blood sampling. To use Accuvein to improve the effectiveness of placing peripheral IV catheter. Accuvein will be used to facilitate peripheral IV catheter placement. Outcome Measures. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Try the modernized ClinicalTrials. Learn more about the modernization effort. Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information.

Search for terms. Save this study. Warning You have reached the maximum number of saved studies Listing a study does not mean it has been evaluated by the U. Federal Government. It can be easily cleaned, and requires no calibration or adjustment. It does not require any contact with the patient.

Second time is completion of marking by ultrasound if necessary. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.

To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies. Try the modernized ClinicalTrials.

Learn more about the modernization effort. Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information. Search for terms. Save this study. Warning You have reached the maximum number of saved studies Listing a study does not mean it has been evaluated by the U.

For general information, Learn About Clinical Studies. Try the modernized ClinicalTrials. Learn more about the modernization effort. Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information.

Search for terms. Save this study. Warning You have reached the maximum number of saved studies Listing a study does not mean it has been evaluated by the U.

Federal Government. Read our disclaimer for details. Results First Posted : April 23, Last Update Posted : April 23, Study Description. No patient identifiers will be collected. Detailed Description:. Study Recruitment and protocol Potential subjects will be patients age months recruited from the pediatric emergency department at Harbor-UCLA.

The patients will be screened for meeting criteria of age months, requiring IV access, not requiring emergent resuscitative access, and not being a ward of the state. Nurses who work in the pediatric emergency department and who obtain IV access in children will be solicited by members of the research team to participate in the study.

All nurses who are trained to use the device will be able to participate as operators in the study. The patient will be enrolled as a subject and the data collection form will be filled out by a trained observer. The data collection form contains: trained observer level of training; blinded nursing number; randomization number; patient gender, age in months, weight, height, Fitzpatrick skin color, dehydration status, mental status, gestational age, chronic medical conditions, and hospitalizations in last two years; nurse's assessment of vein palpability, visibility, and subjective difficulty; nurse's pediatric ED experience and overall experience in years; access tool and whether crossover was utilized; IV gauge, IV access site, number of persons needed to assist, and whether access was successful.

All trained observers will have undergone training to ensure reliability between observers. Once a patient has been identified as a potential subject by the trained observer and consent has been obtained, a blinded randomized manila envelope will be chosen.

The data collection form will be completed by the trained observer and then the nurse will attempt first IV attempt per the arm of the study standard versus with AV assistance.