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Effectiveness of Dry Needling in Shortened Triceps Surae Muscle (DN-TS)

U

Universidad de León

Status

Completed

Conditions

Trigger Point Pain, Myofascial
Myofascial Pain Syndrome

Treatments

Other: Ischemic compression
Other: Dry needling

Study type

Interventional

Funder types

Other

Identifiers

NCT03273985
DN-TS-UCM

Details and patient eligibility

About

To date, there are not studies about the effectiveness of dry needling versus ischemic compression in the triceps surae trigger points. A randomized clinical trial is carried out. A sample of 30 subjects are recruited and allocated into dry needling (n = 15) and ischemic compression (n = 15). Outcome measurements such as dorsal flexion range of motion, plantar pressures, temperature, superficial muscle activity and trigger points pressure pain threshold are measured immediately before and after treatment.

Enrollment

30 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Myofascial pain syndrome in the triceps surae muscle, limitation of ankle dorsal flexion range of motion.

Exclusion criteria

  • Neurologic disorders, pharmacologic treatment (within the previous 3 months), cognitive impairment, prosthesis in the lower limb, systemic or infectious diseases, autoimmune diseases, fibromyalgia, hypothyroidism, anticoagulants or antiplatelet agents, and fear of needles.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Dry needling
Experimental group
Treatment:
Other: Dry needling
Ischemic compression
Experimental group
Treatment:
Other: Ischemic compression

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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