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Peripheral nerve blocks for coccydynia pain

Posterior tibial nerve blocks for the treatment of coccydynia pain: A Prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036418
Enrollment
30
Registered
2021-09-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G549- Nerve root and plexus disorder, unspecified

Interventions

Intervention1: posterior tibial nerve blocks in the treatment of coccidynia pain: 0.3% lignocaine with 20mg of triamcilone in 5ml volume (Totally patient will receive 40mg of triamcilone with 10ml of

Sponsors

AIIMS Rishikesh
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of bilateral posterior tibial nerve blocks in the treatment of coccidynia pain in terms of 1.Pain relief as assessed by Numerical Rating Scale (NRS) on a scale of 1-10 (Annexure I) 2.Global Perceived Effects (Annexure-II) 3.Physical functioning as assessed by Modified Oswestry Disability scale (Annexure â??III) Timepoint: Immediately after the procedure 15 days after the procedure 1 month after the procedure 2 months after the procedure 3 months after the procedure

Secondary

MeasureTime frame
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 at 15 days at 1 month at 2 month at 3 month after the procedure

Countries

India

Contacts

Public ContactPRAVEEN TALAWAR

All India Institute of Medical Sciences, Rishikesh

praveenrt64@gmail.com9654162941

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026