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Clinical Trials/IRCT2016080829269N1
IRCT2016080829269N1
Completed
未知

Study of effect and comparison of two therapeutic exercise protocols on functional outcomes and pain relief in athletes with long - standing adductor – related groin pain

Research Assistance of Faculty of Rehabilitation, Tehran University of Medical Science0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
chronic groin pain.
Sponsor
Research Assistance of Faculty of Rehabilitation, Tehran University of Medical Science
Enrollment
60
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Research Assistance of Faculty of Rehabilitation, Tehran University of Medical Science

Eligibility Criteria

Inclusion Criteria

  • inclusion criteria:the subjects should be male; suffering from groin pain at hip adductor tendon region; between 18\-35 years old; The pain should be chronic with the previous history of minimum two months and accompanied with sport activities; The participants should be of those who are continuing their sport activities more or less; During squeeze test and maximum isometric contraction of hip adductors, they should feel pain that its severity according to VAS must not be more than 5; they should have at least two of following symptoms: a history of morning groin pain and stiffness, nighttime groin pain and groin pain while coughing and sneezing.
  • Exclusion criteria: inguinal or femoral hernia; prostatitis, urinary tract chronic disorders; referential pain due to 10th thoracic down to 5th lumbar segment; malignant disorders; fracture in pelvis or lower limbs; other injuries of lower limbs; ilioinguinal, genitofemoral and lateral femoral cutaneous nerve entrapment; bursitis; osteoarthritis or any other hip joint disorders( according to clinical findings and previous history reported by the subjects); trigger points in adductor muscles belly; NSAID consumption during the study; Lack of cooperation and inability to do therapeutic protocols or to participate in assessments.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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