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Efficacy of laser on knee Arthrosis

Efficacy of low level laser on knee osteoarthritis treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201010104549N2
Enrollment
36
Registered
2010-10-24
Start date
2009-09-29
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis of the knee joint. Primary arthrosis of other joints

Interventions

Intervention 1: The standard treatment that applied to the each of two groups was 1-A 1 MHz continous mode Ultrasound with applicator cross section of 0/8 cm2 in medial and lateral aspect of joint lin
Rehabilitation
The standard treatment that applied to the each of two groups was 1-A 1 MHz continous mode Ultrasound with applicator cross section of 0/8 cm2 in medial and lateral aspect of joint line, duration of 5
The standard treatment that applied for the control group was 1-A 1 MHz continous mode Ultrasound with applicator cross section of 0/8 cm2 in medial and lateral aspect of joint line, duration of 5 mi

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Presence of Idiopathic unilateral knee OA, age 45-75 years, ability of walking, having local pain in the knee region that was greater than 5 with regard to VAS and greater than 48 with regard to the WOMAC scale, Exclusion criteria: having other disorders of knee, affecting hip and ankle joints, lumbar spine pathology, presence of intra-articular effusion, past history of physical therapy or injection into the joint space since 6 months ago, presence of any infection, active bleeding, past history of knee joint surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain at rest. Timepoint: before first session and after tenth session. Method of measurement: on basis of VAS.;Duration of morning stiffness. Timepoint: in the onset of first session and after the final session. Method of measurement: recording of the duration via the patients at minute and quastion of their.;Active Kee flexion Range of Motion. Timepoint: onset of first session and after the tenth session. Method of measurement: via the goniometer by therapist.;Quality of life. Timepoint: onset of first session and after the tenth session. Method of measurement: via questioning of patients on the basis of WOMAC index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasool Bagheri

Tarbiat Modares University of Tehran

rasool.bagheri@ymail.com+98 23 1446 1580

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026