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Clinical Trials/NCT06175533
NCT06175533CompletedNot Applicable

Decrease in Pain Score After Ultrasound Guided CRF for Chronic Plantar Fasciitis Not Responding to Treatment in Addition to Ultrasound Changes

Iraqi Board of medical specialties1 site in 1 country30 target enrollmentStarted: December 1, 2023Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
reduction in pain score
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

detailed changes after ultrasound guided cry for plantar fasciitis in regard pain score and plantar fascia AP diameter in ultrasound scan pre and 30 days post operation

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •chronic plantar fasciitis not responding to treatment not responding to classical injection

Exclusion Criteria

  • •torn plantar fascia

Arms & Interventions

plantar fasciitis

Experimental

Intervention: ultrasound guided 60 degree CRF for plantar fasciitis (Procedure)

Outcomes

Primary Outcomes

reduction in pain score

Time Frame: 6 months

reduction in pain score immediate and 1 week and 2 month according to NAS

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Iraqi Board of medical specialties
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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