Pain and patient-reported outcome associated with surgery for carpal tunnel syndrome or trigger finger under local anesthesia with and without tourniquet

Pain and patient-reported outcome associated with surgery for carpal tunnel syndrome or trigger finger under local anesthesia with and without tourniquet - CTR or TFR with or without tourniquet

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON48016

Enrollment

140

Registered

2019-04-19

Start date

2019-05-18

Completion date

Unknown

Last updated

2024-04-15

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

Conditions

Carpale tunnel syndroom, tenovaginitis stenosans 1.) Carpal tunnel syndrome median neuropathy. 2.) Stenosing tenosynovitis trigger finger

Interventions

Application of a tourniquet during regular surgery

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Operative treatment for carpal tunnel syndrome or stenosing tenosynovitis

Exclusion criteria

Exclusion criteria: Coagulopathy or use of vitamin K antagonist that may not be temporary withdrawn Recurrent or persisting CTS or TVS Axillary lymph node dissection of the affected limb

Design outcomes

Primary

Measure	Time frame
Pain during the surgery on a 0-10 numeric rating scale	—

Secondary

Measure	Time frame
Patient-reported outcome measures: - QuickDASH - BCTQ - Postoperative complications	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)