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Laser Therapy, Pain and Carpometacarpal Joint Osteoarthritis Treatment

U

University of Malaga

Status

Completed

Conditions

Thumb Osteoarthritis
Physical Disorder
Pain

Treatments

Other: Laser
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03270488
UMalaga2

Details and patient eligibility

About

Osteoarthritis (OA) is a chronic and prevalent joint disorder with great impact on quality of life and high economic burden. Although a number of conservative therapies have proven to be effective for the management of hand OA, only modest treatment effects were reported for most individual interventions. The aim of the proposed study is to assess the effect of laser therapy on pain, function and force in patients with carpometacarpal osteoarthritis (CMC OA).

Full description

A randomized, controlled, single-center, double-blind, clinical trial, with 1:1 allocation ratio, were carried out involving patients diagnosis of CMC joint OA grade 1-2 (aged 18 years and above). Both assessor and statistician remained blinded. The research diagnostic criteria for carpometacarpal joint osteoarthritis was used to assess all individuals who agree to participate. All participants were submitted to a clinical examination and X-ray assessment of thumb base to determine carpometacarpal osteoarthritis grade. Based on the clinical and radiological findings, the participants were classified by a rheumatology. Those with CMC OA grade 2-3 were included in the study. The experimental group received laser therapy and control group received a placebo treatment.

The primary outcome measures was pain scores during daily living activities (DLA)- at the base of the thumb measured with VAS (Unidimensional measure of pain: 0-10 (0, no pain and 10, worst pain), and changes in hand function measured using the Quick-Dash questionnaire. Secondary outcome measures included changes in pinch strength. All outcome measures were collected at baseline, immediately following the intervention at 4 weeks and at 12 weeks following the end of the intervention.

Enrollment

61 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women over 18 diagnosis of CMC joint OA in their dominan hand.
  • State 1-2 according to the American College of Rheumatology.
  • Pain intensity during activities of daily living (ADLs) of up to 4 of 10 on the visual analog scale (VAS)
  • Ability to read or understand the patient information sheets.
  • Ability to sign a consent form will be included in the study

Exclusion criteria

  • Neurologic disorder affecting the upper limb
  • Previous treatment for their hand problem in the last 6 months including an intra-articular joint injection to wrist, fingers, or thumb
  • Had fractures or a significant hand injury or previous surgery to the wrist, thumb or hand
  • Finger tenosynovitis.
  • Dupuytren disease.
  • Psychological treatment.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

61 participants in 2 patient groups, including a placebo group

Laser Group
Experimental group
Description:
Laser application three times a week for 4 weeks.
Treatment:
Other: Laser
Placebo group
Placebo Comparator group
Description:
The same equipment was used with a pen that emits a red guide light and a warning sound, but without the emission of a laser beam.
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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