NCT00775554

Brief Summary

Will use visual analog scales to compare effectiveness of traditional hematoma block vs ultrasound guided hematoma block with regards to pain. This will be done for closed forearm fractures.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2008

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

October 17, 2008

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 20, 2008

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2009

Completed
Last Updated

October 14, 2015

Status Verified

October 1, 2008

Enrollment Period

11 months

First QC Date

October 17, 2008

Last Update Submit

October 13, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • Visual analog scale movement

Study Arms (2)

traditional hematoma block

OTHER

people will receive traditional hematoma block for closed forearm fractures

Other: ultrasound guided hematoma block

ultrasound guided hematoma block

OTHER

pts. will receive a hematoma block using bedside ultrasound to guide the placement

Other: ultrasound guided hematoma block

Interventions

pt. will receive ultrasound guided hematoma block

Also known as: ultrasound
traditional hematoma block

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age \> 18
  • Closed forearm fracture

You may not qualify if:

  • Mentally impaired, visually impaired or deaf
  • Age \< 18
  • Alcohol on board

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

St. Luke's Roosevelt Hospital

New York, New York, 10025, United States

Location

MeSH Terms

Interventions

High-Energy Shock Waves

Intervention Hierarchy (Ancestors)

Ultrasonic WavesSoundRadiation, NonionizingRadiationPhysical Phenomena
0

Study Design

Study Type
interventional
Phase
not applicable
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 17, 2008

First Posted

October 20, 2008

Study Start

September 1, 2008

Primary Completion

August 1, 2009

Last Updated

October 14, 2015

Record last verified: 2008-10

Locations