- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01253863
Diagnostic Accuracy of the Preoperative Clinical Examination in Upper Limb Injuries
December 2, 2010 updated by: Isfahan University of Medical Sciences
Study of Accuracy of Preoperative Examination in Penetrating Wound
The purpose of this study is to determine the accuracy of preoperative clinical examination in penetrating injuries
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Penetrating injuries is a common cause of severe neurovascular damage, both in adults and children.we
evaluated the accuracy of the preoperative clinical examination in depicting lesions caused by penetrating wounds of hands or forearms.
Study Type
Interventional
Enrollment (Actual)
250
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Isfahan, Iran, Islamic Republic of
- Al-Zahra University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Deep penetrating injury to upper limb
Exclusion Criteria:
none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: determining damaged tissue
|
exploration of wound for determining damaged tissue
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of determined tendon
Time Frame: 5 min after admission
|
we evalauted tendon injuries without exploration of wound
|
5 min after admission
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of determined injured nerves
Time Frame: 5 min after admision
|
we evaluated the number of detemined injured nerves without exploration of wound
|
5 min after admision
|
|
number of damaged arteries
Time Frame: 5 min after admission
|
we evaluated the number of detemined injured arteries without exploration of wound
|
5 min after admission
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: hamidreza shemshaki, MD, research comittee
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2006
Primary Completion (Actual)
May 1, 2008
Study Completion (Actual)
September 1, 2009
Study Registration Dates
First Submitted
December 2, 2010
First Submitted That Met QC Criteria
December 2, 2010
First Posted (Estimate)
December 3, 2010
Study Record Updates
Last Update Posted (Estimate)
December 3, 2010
Last Update Submitted That Met QC Criteria
December 2, 2010
Last Verified
August 1, 2006
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ASD-1213-7
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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