Clinical TrialID 2118

Cortisone Injection vs Trigger Point Dry Needling Fin the Treatment of Greater Trochanter Pain Syndrome: A Pilot Study

NCT02639039

Hip Injuries

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Record Fields

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Clinical Trial Id
2118
Evidence Id
2118
Core Evidence Id
2118
Source Clinical Trial Id
2089
Herb2 Clinical Trial Id
HBCT002089
Nct Id
NCT02639039
Title
Cortisone Injection vs Trigger Point Dry Needling Fin the Treatment of Greater Trochanter Pain Syndrome: A Pilot Study
Status
Completed
Phase
Phase 4
Study Result
No
Study Condition
Hip Injuries
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (PARTICIPANT)|Primary Purpose: TREATMENT
Intervention
DRUG: Cortisone Injection|PROCEDURE: Trigger Point Dry Needling
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Single
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
50
Outcome Measure
Participants change in pain rating scores from baseline to 6 weeks will be accessed., Baseline and 6 weeks|Patient specific function score (PSPS) from baseline to 6 weeks will be accessed., Baseline and 6 weeks
Sponsor Collaborator
Scott and White Hospital & Clinic
Funded By
OTHER
Location
Other Id
110495
Start Date
2013-02
Primary Completion Date
2015-07
Completion Date
2015-07
First Posted
2015-12-24
Results First Posted
Last Update Posted
2015-12-29
Study Document
Study Url
https://clinicaltrials.gov/study/NCT02639039
Title Cn
Title En
Cortisone Injection vs Trigger Point Dry Needling Fin the Treatment of Greater Trochanter Pain Syndrome: A Pilot Study
Bilingual Status
semi_complete