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Saphenus blok reduceerd opname duur na epifysiodese van de knie - een triple blind superiority trial

Conditions
We include 44 patients (22 verum 22 placebo) who have to ondergoe percutan epiphysiodesis of both knees under gerneal anesthesia.epifysiodesesaphenus blok
Registration Number
NL-OMON22187
Lead Sponsor
Wilhelmina Ziekenhuis Assen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

12-18 yaers of age

ASA 1 of 2

Exclusion Criteria

ASA 3 or higher

chronic pain

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
lenght of stay after surgery
Secondary Outcome Measures
NameTimeMethod
intra- and postoperative opiod consumption<br /><br>NRS pain scores<br /><br>time in the post anesthetic care unit<br /><br>time to walk (with crutches)<br /><br>strength of the quadriceps muscle<br /><br>overall patient satisfaction
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