Clinical Trials Directory

Trials / Completed

CompletedNCT05237492

The Influence of Tramadol on Platelet Function

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Medical University of Graz · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The aim of this ex-vivo study is to quantify the effect of tramadol on platelet aggregation.

Detailed description

The aim of this study is to quantify the effect of tramadol on platelet aggregation. To this end, the effect of tramadol on platelet function will be demonstrated in an ex-vivo study using optical aggregometry (LTA) on whole blood of 15 patients. The main objective variable is to use platelet function assays (LTA) as well as thrombelastography (TEG) to determine this effect on platelet function. The null hypothesis of this study is that tramadol does not affect platelet aggregation in healthy patients. In addition, two further questions will be addressed: * using a titration series, to attempt to plot a dose/response curve of the effect of tramadol on platelet function. * tramadol is often administered together with other drugs such as NSAIDs (ibuprofen), novalgin, SSRIs or other opioids such as morphine or in the surgical setting fentanyl and remifentanil. A series of studies will be conducted to determine whether these combinations alter the effect of tramadol on platelet function.

Conditions

Interventions

TypeNameDescription
DRUGTramadolBlood samples will be drawn from 15 patients. Tramadol will be added to all this samples in-vitro and its influence on platelets´ function will be measured.

Timeline

Start date
2022-01-26
Primary completion
2023-07-15
Completion
2023-07-15
First posted
2022-02-14
Last updated
2024-01-18

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT05237492. Inclusion in this directory is not an endorsement.