Ultrasound Guided Ganglion Impar Block
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBaşakşehir Çam & Sakura City Hospital
The aim of this study is to evaluate feasibility, reliability and short term effectiveness of ganglion impar block with ultrasound in patients with chronic coccygodinia.
Age between 18-65 years.
Coccydynia persisting for at least three months.
Being scheduled for a ganglion impar block in the pain medicine outpatient clinic.
Having inadequate response to medical and conservative treatments.
Local infection at the injection site.
Bleeding disorders or diseases and drugs that may cause bleeding diatesis (e.g. renal failure, liver failure, anticoagulant treatments)
History of allergic reaction to the medications to be used.
Pregnancy