- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07666061
Laser vs Lontophoresis in KOA
June 18, 2026 updated by: Abdulaziz Fahad Ahmed Alsulaimani, Kafrelsheikh University
Effectiveness of Laser Therapy Versus Lontophoresis in the Management of Knee Osteoarthritis: A Randomized Controlled Trial
This randomized controlled trial aims to compare the effectiveness of laser therapy and iontophoresis in patients with knee osteoarthritis.
The study will evaluate pain reduction, functional improvement, and knee joint mobility following
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Participants will be randomly assigned into three groups receiving either laser therapy plus conventional physiotherapy, iontophoresis plus conventional physiotherapy, or conventional physiotherapy alone.
Outcome measures will be assessed before and after treatment
Study Type
Interventional
Enrollment (Estimated)
66
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: abdulaziz fahad alsulaimani, MASTER
- Phone Number: 966566613748
- Email: azoztaif88@hotmail.com
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
* Age 45-65 years.
- Diagnosed primary knee osteoarthritis (Grade I-II).
- Both genders.
- Ability to follow treatment protocol.
Exclusion Criteria:
* Previous knee surgery.
- Intra-articular injections within last 6 months.
- Pacemaker.
- Skin lesions at treatment area.
- Severe neurological or cardiovascular disorders.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group A:
Low-Level Laser Therapy
|
Low-level laser therapy combined with conventional physical therapy for patients with knee osteoarthritis to reduce pain and improve functional mobility and knee joint range of motion
Conventional physical therapy program for patients with knee osteoarthritis including therapeutic exercises, stretching, strengthening exercises, and pain relief modalities to improve knee function and mobility.
|
|
Active Comparator: Group B
Iontophoresis
|
Conventional physical therapy program for patients with knee osteoarthritis including therapeutic exercises, stretching, strengthening exercises, and pain relief modalities to improve knee function and mobility.
Iontophoresis using dexamethasone combined with conventional physical therapy for patients with knee osteoarthritis to reduce pain and improve physical function and knee joint mobility
|
|
Active Comparator: Group C
Conventional Physical Therapy Only
|
Conventional physical therapy program for patients with knee osteoarthritis including therapeutic exercises, stretching, strengthening exercises, and pain relief modalities to improve knee function and mobility.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Pain intensity measured using Visual Analogue Scale (VAS)
Time Frame: Baseline and after 4 weeks of treatment
|
Baseline and after 4 weeks of treatment
|
|
Functional disability measured using WOMAC.
Time Frame: Baseline and after 4 weeks of treatment
|
Baseline and after 4 weeks of treatment
|
|
3. Knee Range of Motion (ROM).
Time Frame: Baseline and after 4 weeks of treatment
|
Baseline and after 4 weeks of treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in physical function assessed by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Physical Function Subscale
Time Frame: Baseline (Day 0) and Week 4
|
The WOMAC Physical Function Subscale consists of 17 items assessing difficulty in performing daily activities.
Scores range from 0 to 68, with higher scores indicating worse physical function.
|
Baseline (Day 0) and Week 4
|
|
2. Reduction of joint stiffness.
Time Frame: Baseline and after 4 weeks of treatment
|
Baseline and after 4 weeks of treatment
|
|
|
Change in daily activities performance assessed by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Physical Function Subscale
Time Frame: Baseline (Day 0) and Week 4
|
The WOMAC Physical Function Subscale consists of 17 items assessing difficulty in activities of daily living.
Scores range from 0 to 68, with higher scores indicating worse functional limitation.
|
Baseline (Day 0) and Week 4
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: hane mohamed hamed, PHD, professor of orthopedic surgery depaetment of orthopedic surgery faculty of medicine kafrelsheikh university
- Study Chair: mahmoud mohamed ewida, PHD, professor of basic sciences for physical therapy department of basic sciences for physical therapy faculty oh physical therapy kafrelsheikh university
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 (Estimated)
August 1, 2026
Primary Completion (Estimated)
October 30, 2026
Study Completion (Estimated)
April 1, 2027
Study Registration Dates
First Submitted
June 12, 2026
First Submitted That Met QC Criteria
June 18, 2026
First Posted (Actual)
June 24, 2026
Study Record Updates
Last Update Posted (Actual)
June 24, 2026
Last Update Submitted That Met QC Criteria
June 18, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KFSIRB200-1047
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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