Condition: Carpal Tunnel Syndrome · Sponsor: Kuopio University Hospital
Carpal tunnel syndrome (CTS) is the most commonly appearing entrapment neuropathy of the upper extremity. Treatment options include both non-operative and operative methods. Surgical treatment, carpal tunnel release (CTR), involves division of the transverse carpal ligament. Surgery can be performed under axillary or intravenous block, or general anaesthesia. There are no prior randomised controlled trials (RCT) comparing local infiltration anaesthesia to local infiltration anaesthesia augmented with a distal median nerve block in CTR. The aim of this trial is to investigate whether adding a distal median nerve block to local anaesthesia reduces the patient's perceived pain level for up to 72 hours after CTR, compared to using only local anaesthesia, i.e., an anaesthesia mixture injected solely in and around the planned incision and nerve release. The null hypothesis is that the use of distal median nerve block with local anaesthesia does not reduce pain after CTR compared to pure local anaesthesia. PERSONNEL (carPal tunnEl ReleaSe lOcal iNfiltratioN mEdian bLockade) is a double-blinded, i.e., patient and investigators, RCT in patients with CTS. Patients will be randomly divided into two parallel trial groups, 1:1 in size to each other. Fifty-nine patients will be needed for each group to have adequate power. The primary outcome is the pain level perceived by the patient after the procedure during the first 72 hours using the Visual Analogue Scale (VAS). Secondary outcomes …
This description comes directly from the study's public registry record.
Noora Heikkinen, MBBS · +358504421930 · noorheik@student.uef.fi
Yrjänä Nietosvaara, Prof. · +358447176883 · yrjana.nietosvaara@pshyvinvointialue.fi
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| Kuopio University hospital, Department of Orthopaedics, Traumatology and Hand Surgery | Kuopio, Northern Savonia, Finland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05372393