Ultrasound Guidance for Intravenous Cannulation in Emergency Department Patients.
This study has been completed.
Sponsor:
University of California, San Francisco
Information provided by:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT00692549
First received: June 4, 2008
Last updated: June 5, 2008
Last verified: June 2008
| Tracking Information | |
|---|---|
| First Received Date ICMJE | June 4, 2008 |
| Last Updated Date | June 5, 2008 |
| Start Date ICMJE | June 2005 |
| Primary Completion Date | August 2005 (final data collection date for primary outcome measure) |
| Current Primary Outcome Measures ICMJE |
Number of IV Attempts [ Designated as safety issue: Yes ] |
| Original Primary Outcome Measures ICMJE | Same as current |
| Change History | Complete list of historical versions of study NCT00692549 on ClinicalTrials.gov Archive Site |
| Current Secondary Outcome Measures ICMJE |
Time to placement of IV catheter [ Designated as safety issue: Yes ] |
| Original Secondary Outcome Measures ICMJE | Same as current |
| Current Other Outcome Measures ICMJE | Not Provided |
| Original Other Outcome Measures ICMJE | Not Provided |
| Descriptive Information | |
| Brief Title ICMJE | Ultrasound Guidance for Intravenous Cannulation in Emergency Department Patients. |
| Official Title ICMJE | Ultrasound-Guided Peripheral Intravenous Cannulation in Emergency Department Patients With Difficult IV Access: a Randomized Trial. |
| Brief Summary | A randomized trial of the use of ultrasound by emergency physicians in the placement of intravenous catheters in emergency patients who are found to have difficult intravenous access (defined as two failed attempts by nursing staff). |
| Detailed Description | Not Provided |
| Study Type ICMJE | Interventional |
| Study Phase | Not Provided |
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Safety Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Condition ICMJE | Difficult IV Access |
| Intervention ICMJE | Device: ultrasound |
| Study Arm (s) |
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| Publications * | Not Provided |
|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
|
| Recruitment Information | |
| Recruitment Status ICMJE | Completed |
| Enrollment ICMJE | 60 |
| Completion Date | August 2005 |
| Primary Completion Date | August 2005 (final data collection date for primary outcome measure) |
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
|
| Gender | Both |
| Ages | 18 Years and older |
| Accepts Healthy Volunteers | No |
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects |
| Location Countries ICMJE | United States |
| Administrative Information | |
| NCT Number ICMJE | NCT00692549 |
| Other Study ID Numbers ICMJE | RandomizedIVUS |
| Has Data Monitoring Committee | No |
| Responsible Party | John C. Stein MD, University of California, San Francisco |
| Study Sponsor ICMJE | University of California, San Francisco |
| Collaborators ICMJE | Not Provided |
| Investigators ICMJE | Not Provided |
| Information Provided By | University of California, San Francisco |
| Verification Date | June 2008 |
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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