Significant Pathology Associated With Crossed Leg Sign
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Purpose
By determining the correlation of a Crossed Leg Sign with signifcant pathology, a clinician would then be able to use this correlation to risk stratify his/her patients for significant pathology.
| Condition |
|---|
|
Pathology |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Crossed Leg Sign and it's Correlation With Significant Pathology |
| Estimated Enrollment: | 400 |
| Study Start Date: | May 2012 |
| Estimated Study Completion Date: | February 2013 |
| Estimated Primary Completion Date: | February 2013 (Final data collection date for primary outcome measure) |
By determining the correlation of a Crossed Leg Sign with signifcant pathology, a clinician would then be able to use this correlation to risk stratify his/her patients for significant pathology. Therefore, by determining the sensitivity and specificity of this physical exam finding, the clinician would have a better idea of the patients clinical management, including diagnostic testing and ultimate treatment of the patient. Crossed Leg Sign will be defined in this study as: any patient observed in the Emergency Department with sustained crossed legs. To my knowledge, crossed legs have never been evaluated in regards to it's correlation with significant pathology. This could potentially add another physical exam finding to be used by the clinician.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
This study should include all comers. To exclude a patient population would add a selection bias.
Inclusion Criteria:
- Any patient observed in the Emergency Department with sustained crossed legs.
Exclusion Criteria:
- Any patient not observed to have sustained crossed legs and is not being used as a control.
Contacts and Locations| Contact: John D Uelk, DO | 314-605-4486 | juelk1@hfhs.org |
| Contact: Michael Ward, DO | 908-930-2405 | mward4@hfhs.org |
| United States, Michigan | |
| Henry Ford Wyandotte Hospital | Not yet recruiting |
| Wyandotte, Michigan, United States, 48192 | |
| Contact: John D Uelk, DO 314-605-4486 juelk1@hfhs.org | |
| Principal Investigator: John D Uelk, DO | |
| Principal Investigator: | John D Uelk, DO | Henry Ford Health System |
More Information
No publications provided
| Responsible Party: | Uelk, J. Daniel, D.O. |
| ClinicalTrials.gov Identifier: | NCT01569555 History of Changes |
| Other Study ID Numbers: | 7286 |
| Study First Received: | March 30, 2012 |
| Last Updated: | March 30, 2012 |
| Health Authority: | United States: Federal Government |
ClinicalTrials.gov processed this record on May 22, 2013