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Clinical Trials/NCT04731350
NCT04731350CompletedNot Applicable

Effect of Extra Corporeal Shock Wave Versus Dexamethasone Iontophoresis in Treatment of Knee Osteoarthritis

Cairo University1 site in 1 country60 target enrollmentStarted: January 20, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
visual analogue scale (VAS)

Study Overview

Brief Summary

Both extra corporeal shock wave and dexamethasone iontophoresisare effective in treatment of knee osteoarthritis but which one is more effective is not clear yet . so the purpose of this study was to investigate and compare between the effect of shock wave and iontophoresis in treatment of knee osteoarthritis . it was hypothesized that there will be no difference between the effect of shock wave and iontophoresis on treatment of knee osteoarthritis.

Detailed Description

60 subjects with grade II knee osteoarthritis will be recruited from outpatient clinic of faculty of physical therapy and then they will be assigned randomly by sealed envelope into three groups ;group A (shock wave group) will received radial extracorporeal shock wave ,group B (Iontophoresis group ) will receive deaxamthasone iontophoresis and group c (control group) will receive traditional tratment ( stregnthening exerciseces) all treatment will be once session per week for four weeks .pain intensity ,knee ROM and knee injury and osteoarthritis outcome score physical function short (KOOS-PS).

Study Design

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

Eligibility Criteria

Ages
40 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Symptomatic knee OA for at least 3 months according to clinical criteria of American College of Rheumatology
  • •Radiologic findings had to be compatible with knee OA, with kelgren and Lawrence (K-L) grade 2 in a simple X ray .
  • •Tenderness on medial tibial plateau
  • •Intensity of pain: visual analogue scale equal to 5 or greater
  • •Failure of two or more types of previous conservative treatment (medication, anti-inflammatory drugs, physical therapy, stretching, acupuncture, orthotics and others)

Exclusion Criteria

  • •Neuorological and vestibular system disorder, systematic inflammatory disease, steroid injections in the last six months
  • •Any contraindication to magnetic resonance imaging or radiography, or trauma history on knee
  • •history of previous knee surgery -

Arms & Interventions

Shock wave(A)

Experimental

subjects will recive radial extracorporeal shock wave (2000 shock/session, 10Hz and EFD 0.178 mJ/mm²) on knee joints once per week for four weeks in addition to strengthening exercise

Intervention: radial extracorporeal shock wave (Device)

Shock wave(A)

Experimental

subjects will recive radial extracorporeal shock wave (2000 shock/session, 10Hz and EFD 0.178 mJ/mm²) on knee joints once per week for four weeks in addition to strengthening exercise

Intervention: Exercise (Other)

Iontophoresis (B)

Experimental

subjects will recive dexamethasone iontophoresis on knee joints once per week for four weeks in addition to strengthening exercise

Intervention: iontophoresis (Device)

Iontophoresis (B)

Experimental

subjects will recive dexamethasone iontophoresis on knee joints once per week for four weeks in addition to strengthening exercise

Intervention: Exercise (Other)

Control (C)

Other

stregnthening exercise;straight leg raising exercisein which the patients were positioned in the crook lying position with the unexercised limb was the flexed one then the patients were asked to contract the quadriceps muscle and elevate the limb to 45º and hold for 6 seconds, slowly lower the limb and then relax for 6 seconds, three sets of 10 repetitions were don ,Isometric quadriceps contraction (quadriceps drill) in full knee extension maintained for 5 seconds, followed by a 5-second rest; the exercise was performed for 20 repetitions per session .treatment once per week for four weeks

Intervention: Exercise (Other)

Outcomes

Primary Outcomes

visual analogue scale (VAS)

Time Frame: change from baseline to immediately pre treatment and from pre treatment to immediately post treatment

pain intensity will be assessed by using visual analogue scale

Secondary Outcomes

  • knee injury and osteoarthritis outcome score physical function short (KOOS-PS)(change from baseline to immediately pre treatment and from pre treatment to immediately post treatment)
  • knee range of motion (ROM)(change from baseline to immediately pre treatment and from pre treatment to immediately post treatment)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shimaa Taha Abu El Kasem

principle investigator

Cairo University

Study Sites (1)

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