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Clinical Trials/IRCT20220804055615N3
IRCT20220804055615N3
Recruiting
Phase 1

Effects of trigger point dry needling among patients with anterior knee pain

Memon College of Physical and Rehasbilitaive Medicine0 sites30 target enrollmentTBD
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ConditionsAnterior knee pain.ICD-10 code M25. 569 for Pain in unspecified knee is a medical classification as listed by WHO under the range - ArthropathiesM25.569

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Anterior knee pain.
Sponsor
Memon College of Physical and Rehasbilitaive Medicine
Enrollment
30
Status
Recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
Memon College of Physical and Rehasbilitaive Medicine

Eligibility Criteria

Inclusion Criteria

  • •Male with age between 20 to 45 years
  • •Subjects having anterior knee pain
  • •Subjects with myofasical trigger points in quadriceps muscle

Exclusion Criteria

  • •Patients taking anticoagulant medications
  • •Patients with meniscal tears, patellar tendinopathy , ligamentous injury
  • •Patients with knee osteoarthritis
  • •Patients with lumbosacral nerve root or peripheral nerve involvement
  • •Patients having a history of prior knee surgery
  • •Patients who had received acupuncture, dry needling or injection for knee pain during the past 6 months

Outcomes

Primary Outcomes

Not specified

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