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Evaluation the influence of the local low-power laser therapy in patients with avascular necrosis of femoral head ?

Evaluation the effects? of the local low-power laser therapy on clinical and imaging alterations in patients with avascular necrosis of femoral head

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180305038955N1
Enrollment
32
Registered
2018-07-25
Start date
2018-07-23
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Avascular Necrosis of Femoral Head. Osteonecrosis due to drugs, unspecified femur

Interventions

In this study, the laser fluence (energy) is transmitted through the skin to the anatomical location of the affected hip (15 points for each joint). The periods of radiations include 9 courses (each c

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients from both sexes were entered into the study with grade 1 and 2 on the basis of the American Society of Anesthesiology criteria. The participants were diagnosed as avascular necrosis of femoral head ?(grade 3-4) based on the diagnostic criteria of the Massachusetts hospital. Age range 18-40 years

Exclusion criteria

Exclusion criteria: Patients who tend to have surgery Grade 1,2 ,5 and 6 of American Society of Anesthesiologists (ASA) Radiologic Criteria for Femoral head AVN patients were not intended to be treatde Malignancy in the vicinity of the treatment area Dermatologic problems which makes the treatment impossible Other invasive or Non-invasive treatments on the affected area

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Measure of pain at the beginning of the study (before the intervention) and after each 10-session of treatment period. Method of measurement: Visual Analogue scale (VAS).;Hip motion range. Timepoint: Measure of pain at the beginning of the study (before the intervention) and after each 10-session of treatment period. Method of measurement: Range of Motion.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAliakbar Jafariyan

Iran University of Medical Sciences

aajafari41@gmail.com+98 21 8214 1612

Outcome results

None listed

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