Peripheral nerve blocks for coccydynia pai
Not Applicable
- Conditions
- Health Condition 1: G549- Nerve root and plexus disorder, unspecified
- Registration Number
- CTRI/2021/09/036418
- Lead Sponsor
- AIIMS Rishikesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patient suffering from coccidynia due to any cause, which is not responding to conservative treatment with numerical rating scale of > 4/10
2.Duration of pain >3months
Exclusion Criteria
1.Coagulopathy and/or patients on anticoagulants.
2.Infection at the site of injection.
3.Hypersensitivity to local anesthetic agent
4.History of any major comorbid medical conditions, those interfere with recording of study outcomes, and pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the efficacy of bilateral posterior tibial nerve blocks in the treatment of coccidynia pain in terms of <br/ ><br>1.Pain relief as assessed by Numerical Rating Scale (NRS) on a scale of 1-10 (Annexure I) <br/ ><br>2.Global Perceived Effects (Annexure-II) <br/ ><br>3.Physical functioning as assessed by Modified Oswestry Disability scale (Annexure â??III) <br/ ><br>Timepoint: Immediately after the procedure <br/ ><br>15 days after the procedure <br/ ><br>1 month after the procedure <br/ ><br>2 months after the procedure <br/ ><br>3 months after the procedure
- Secondary Outcome Measures
Name Time Method 1.To assess spontaneous reporting of adverse effects and the incidence of complications due to the procedureTimepoint: complications will be assessed immediately after the procedure <br/ ><br> <br/ ><br>at 15 days <br/ ><br> <br/ ><br>at 1 month <br/ ><br> <br/ ><br>at 2 month <br/ ><br> <br/ ><br>at 3 month after the procedure