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Clinical Trials/NCT01073124
NCT01073124CompletedNot Applicable

Sensitivity of the Saline Load Test With and Without Methylene Blue Dye in the Diagnosis of Traumatic Knee Arthrotomies

United States Naval Medical Center, San Diego1 site in 1 country60 target enrollmentStarted: May 1, 2008Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Volume (mm) injected at time of outflow

Study Overview

Brief Summary

The purpose of this study is to determine if adding blue dye improves the saline load test, which is a way to detect a traumatic intraarticular knee injury by injecting normal saline into the knee and looking for outflow through the wound.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Individuals with diagnosis warranting elective knee arthroscopy

Exclusion Criteria

  • •Pregnant women
  • •Decreased knee range of motion (flex < 125, ext <0)
  • •Active infection of knee joint
  • •history of or current intraarticular knee malignancy
  • •history of open traumatic injury of the knee

Arms & Interventions

Normal Saline

Active Comparator

Normal Saline injected intraarticularly into the knee joint

Intervention: Saline Load Test (Procedure)

Dilute Methylene Blue Dye

Experimental

1 ml methylene blue dye per 500 ml normal saline injected intraarticularly into the knee

Intervention: Saline Load Test (Procedure)

Outcomes

Primary Outcomes

Volume (mm) injected at time of outflow

Time Frame: 1 month

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
United States Naval Medical Center, San Diego
Sponsor Class
Fed
Responsible Party
Sponsor

Study Sites (1)

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