Frequency of Piriformis Syndrome:Does the Presence of One Pathology Rule Out the Other?
1 other identifier
interventional
100
0 countries
N/A
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable chronic-pain
Started Jul 2022
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 21, 2022
CompletedStudy Start
First participant enrolled
July 10, 2022
CompletedFirst Posted
Study publicly available on registry
July 11, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 15, 2022
CompletedJuly 12, 2022
July 1, 2022
5 days
March 21, 2022
July 8, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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
Study Arms (1)
patients with unilateral hip and leg pain
OTHERMusculoskeletal system examination, neurological examination, visual analog scale (VAS) score and DN4 (Douleur Neuropathique 4 Questions) of patients presenting with unilateral hip and/or leg pain, 3 tests frequently used in the diagnosis of priformis (Freiberg test, Pace sign, FADIR) ) will be applied. Patients with suspected priformis syndrome will be given an intramuscular injection If the pain intensity decreases by 50% or more after the intramuscular injection, the diagnosis of piriformis will be made.
Interventions
Priformis intramuscular injection will be administered with 5 cc 2% lidocaine, accompanied by a nerve stimulator under ultrasound guidance
Eligibility Criteria
You may qualify if:
- Patients presenting with unilateral hip and/or leg pain
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
March 21, 2022
First Posted
July 11, 2022
Study Start
July 10, 2022
Primary Completion
July 15, 2022
Study Completion
July 15, 2022
Last Updated
July 12, 2022
Record last verified: 2022-07