Actively Recruiting

Phase Not Applicable
Age: 30Years - 65Years
FEMALE
NCT06406023

Effectiveness of Instrument Assisted Soft Tissue Mobilization in Management of Piriformis Syndrome

Led by Riphah International University · Updated on 2024-05-09

38

Participants Needed

1

Research Sites

24 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to assess the effectiveness of IASTM on pain, ROM, Disability and Quality of life among Piriformis Syndrome patients. This study will add to the growing body of knowledge as there are very limited researches done in Pakistan using IASTM in patients with Piriformis Syndrome.

CONDITIONS

Official Title

Effectiveness of Instrument Assisted Soft Tissue Mobilization in Management of Piriformis Syndrome

Who Can Participate

Age: 30Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed patients of Piriformis syndrome.
  • Only females will be included in this study.
  • Participants aged 30-65 years.
  • Pain due to non-discogenic sciatic nerve entrapment in sub gluteal space.
  • Pain aggravated by prolonged sitting, lying, standing.
  • Positive FAIR test, Pace sign, Laseque sign, Beatty maneuver and Freiberg test.
  • Negative Kemp sign, Milgram's test, Bowstring test, Braggard test and Lasegue differential test.
Not Eligible

You will not qualify if you...

  • Patients with any Intrinsic Etiology such as Haemarthrosis, rheumatoid arthritis or infection.
  • Patients with any recent severe trauma, fractures, subluxation or ligament injury.
  • Malignancy, Open wound Fracture, DVT, Compartment syndrome, Pregnancy.
  • Patients with irreversible nerve damage.
  • Patients with lumbar disc herniation or any disc pathology.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Railway General Hospital

Rawalpindi, Punjab Province, Pakistan

Actively Recruiting

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Research Team

N

Neha Noor, Masters

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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