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ID
Source
Brief title
Health condition
carpal tunnel syndrome
trigger finger
Sponsors and support
Intervention
Outcome measures
Primary outcome
Pain
Secondary outcome
PROMS
Complications
Background summary
To investigate the effect on pain and patient reported outcome measurements with or without a tourniquet in carpal tunnel- and triggerfinger relase. Determine difference in experienced pain during the procedure between those two groups and to determine the effect on recovery and functional outcome in the longer term.
Study objective
There is no difference in perioperative pain between patients with and without a tourniquete
Study design
Pre-operative: PROMS
Peri-operative: pain injection, pain tourniquet, total pain operation
FU 2 weeks: infection, hematoma, dehiscence
FU 6 weeks: PROMS
FU 3 months: PROMS
FU 6 months: PROMS, ultrasound
FU 12 months: PROMS
Intervention
Group 1: patients with tourniquet
Group 2: patients without tourniquet
Procedure (carpal tunnel- and trigger finger release) will be performed according to current operation procotol
Inclusion criteria
all patients with elective carpal tunnel release and triggerfinger release under local anesthesia > 18 years old
Exclusion criteria
- coumarines who cannot be interrupt
- patients with persistent/recurrent carpal tunnel syndrome or trigger finger after previous surgery
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL8499 |
| Other | METC Brabant : METCP1906 |