Reducing pain and discomfort during and after bone marrow aspiratio

Completed

• Conditions: Pijn en angstbeleving; Bone marrow aspiration and biopsy; bone marrow biopsy; 10025309

• Registration Number: NL-OMON42943
• Lead Sponsor: Slotervaartziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2018-11-28
• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 42

Inclusion Criteria

1. Patients with an indication to undergo a first bone marrow aspiration in MC Slotervaart.
2. Age > 18 years
3. Patient is capable to give written informed consent

Exclusion Criteria

1. Known allergy for any of the study medicines
2. Pregnancy
3. In hospital patients

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameters<br /><br>- Visual Analogue Scale (VAS) for pain, directly after the procedure<br /><br>- Visual Analogue Scale (VAS) for anxiety, fear for a next BMAB two weeks after<br /><br>procedure</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary study parameters/endpoints<br /><br>- Fear of Pain Questionnaire-III<br /><br>- VAS for pain and anxiety at other moments than described at the main study<br /><br>parameters<br /><br>- 5 point Likert scale, fear for a BMAB<br /><br>- VAS for discomfort<br /><br>- Possibility to follow instructions during the procedure</p><br>