To assess and compare the intralesional traiamcinolone injection by ultrasound guided vs palpation method in the management of acute plantar fasciitis
Not Applicable
- Conditions
- Health Condition 1: M708- Other soft tissue disorders related to use, overuse and pressure
- Registration Number
- CTRI/2021/08/035846
- Lead Sponsor
- department of anesthesiology and critical care pain medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)asa grade 1 and 2.
2)body weight 45-80 kgs
3)patients who were presented with acute heal pain to the pain clinic on outpatient basis
Exclusion Criteria
1) patients not willing to participate in the study
2) case with diabetes mellitus and immune compromised status
3)history of blood coagulopathies,vsepsis,or other skin infection of local site
4) patient allergic to drug used for study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method mean pain score in-terms of VAS scaleTimepoint: 2nd and 4th week post injection procedure
- Secondary Outcome Measures
Name Time Method mean thickness and the echogenecity in plantar fasciaTimepoint: from baseline to 2 to 4 weeks of post injection period