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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05450913
Other study ID # piriformis
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 10, 2022
Est. completion date July 15, 2022

Study information

Verified date July 2022
Source Diskapi Teaching and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the investigators is to determine the frequency of priformis syndrome in patients presenting with hip and/or leg pain and to investigate the association of Priformis syndrome with other pathologies of the lumbar spine and hip.


Description:

Priformis Syndrome is a neuromuscular disorder characterized by compression or irritation of the sciatic nerve under the piriformis muscle, tenderness in the piriformis muscle, and back, hip, and leg pain. The pain may radiate along the sciatic nerve trace in the gluteal region and posterior thigh. Diagnosis is based on clinical symptoms, specific physical examination findings, and positive response to local injection. The diagnosis of piriformis syndrome is usually made only after lumbar spine pathologies are excluded. This traditional approach leads to underdiagnosis of piriformis syndrome. More than one cause may coexist in hip and/or leg pain.The existence of one cause does not exclude the other.Priformis syndrome should not be a diagnosis of exclusion. In the differential diagnosis of hip and/or leg pain, physical examination to exclude piriformis syndrome and injection of local anesthetic into the piriformis muscle is much less invasive than surgery to confirm lumbar spine pathology and can be performed as an outpatient.Thus, early diagnosis and appropriate treatment process is accelerated. If there is an unfavorable response to the local injection, investigation for lumbar vertebral pathologies can be initiated. The purpose of the investigators under this information and justifications is; To determine the frequency of Priformis syndrome in patients presenting with hip and/or leg pain and to investigate the association of Priformis syndrome with other pathologies of the lumbar spine and hip.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date July 15, 2022
Est. primary completion date July 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Patients presenting with unilateral hip and/or leg pain Exclusion Criteria: - no

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Priformis intramuscular injection with %2 lidocain
Priformis intramuscular injection will be administered with 5 cc 2% lidocaine, accompanied by a nerve stimulator under ultrasound guidance

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Diskapi Teaching and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary To determine the frequency of Priformis syndrome Change in Pain Scores on Visual Analogue Scale scores at 24 hours before and after Priformis muscule injection 1 months
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