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Clinical Trials/NCT03806322
NCT03806322CompletedNot Applicable

A Better Way to Decrease Knee Swelling in Patients With Knee Osteoarthritis: A Single-Blind Randomized Controlled Trial

Marmara University0 sites89 target enrollmentStarted: November 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
89
Primary Endpoint
Pain Intensity

Study Overview

Brief Summary

In this study, we compared the effects of intermittent pneumatic compression along with conventional treatment and cold-pack treatment along with conventional treatment on clinical outcomes in patients with knee osteoarthritis.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
35 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients diagnosed with knee OA according to the criteria of the American College of Rheumatology (ACR), and were considered as stage 2 and 3 according to Kellgren-Lawrence criteria.

Exclusion Criteria

  • •Exclusion criteria were previous knee surgery, malignancy, circulation disorder, and conditions preventing exercise or causing muscle weakness, pregnancy, diagnosis of mental disorder, scar tissue, or metal implants.

Arms & Interventions

Cold-pack Group

Experimental

One group received ultrasound, transcutaneous electrical nerve stimulation, electrical stimulation, exercise, and cold packs

Intervention: Cold-pack (Other)

Intermittent Pneumatic Compression

Experimental

The second group received ultrasound, transcutaneous electrical nerve stimulation, electrical stimulation, exercise, and intermittent pneumatic compression

Intervention: Intermittent Pneumatic Compression (Other)

Outcomes

Primary Outcomes

Pain Intensity

Time Frame: 3 minutes

A Visual Analogue Scale was used to measure pain intensity.

Knee Swelling

Time Frame: 3 minutes

Knee swelling was measured with a tape measure.

Secondary Outcomes

  • Functional Status(10 minutes)
  • Range of Motion(3 minutes)
  • Muscle Strength(10 minutes)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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