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

Withdrawn

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

• Registration Number: NL-OMON39558
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Withdrawn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

Inclusion Criteria

All adult patients (age > 18) who will receive conservative treatment for an extremity fracture.

Exclusion Criteria

Pregnant, breastfeeding or possibly pregnant patients and patients with relevant drug allergies will be excluded from study participation
Further exclusion criteria include: 1) phalangeal fractures; 2) stress fractures; 3) another fracture at any site; 4) pathological fractures; 5) inability to fill out questionnaires; 6) polytrauma patients with other significant injuries outside the skeletal system; 7) patients already receiving any chronic form of analgesic prior to injury; 8) liver or renal dysfunction; 9) diagnosed constipation; 10) patients receiving MAO-inhibitors.

Study & Design

• Study Type: Observational non invasive
• 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>