Pain management after operative treatment of extremity fractures, a randomized clinical trial

Completed

• Conditions: pijn; 10005944; broken bones; Pain after fractures; 10017322

• Registration Number: NL-OMON37699
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

All adult patients (age > 18) who will undergo surgical treatment for an extremity fracture treated in the Academic Medical Center Amsterdam.

Exclusion Criteria

Pregnant, breastfeeding or possibly pregnant patients, patients with relevant drug allergies and children will be excluded from study participation
Further exclusion criteria include: 1) another fracture at any site; 2) pathological fractures; 3) inability to fill out questionnaires; 4) polytrauma patients with other significant injuries outside the skeletal system; 5) patients already receiving any form of analgesic prior to injury; 6) liver or renal dysfunction; 7) diagnosed gastric disease; 8) diagnosed constipation 9) patients receiving MAO-inhibitors.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameters are the outcomes of the pain/satisfaction Numeric<br /><br>Rating Scale.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary study parameters are the outcomes of the self-efficacy scale and<br /><br>the disability questionnaire.</p><br>