Skip to main content
OpenTrials
Completed

NCT Number: NCT02368730

Documentation of the Efficacy of Desmopressin Within the Context of Surgical Procedures

In this non-interventional multicentre, prospective, observational cohort study, the efficacy of desmopressin is evaluated in patients with platelet dysfunction due to acetylsalicylic acid or cox-1-inhibitors within the context of surgical procedures.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Platelet Dysfunction

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Charité - Universitätsmedizin Berlin (there may be other sites in this country)

Berlin, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pre-, peri- or postoperative treatment with a standard dose of desmopressin as a result of platelet dysfunction (disturbance of blood platelet function) due to treatment with acetylsalicylic acid or cox-1-inhibitor.
  • Decision on the therapy with MINIRIN parenteral 4 Microgram/ml solution for injection has already been made independently by the physician beforehand
  • The patients (≥ 18 years) have been informed about the non-interventional study and have given their written consent for participation

Exclusion criteria

  • Participation in a clinical trial
  • Treatment with acetylsalicylic acid for cardiovascular indications

Treatment and study plan

Desmopressin

Drug

Other names: Minirin

Primary outcomes

  1. Change in platelet function pre- and post-administration of desmopressin

    Time frame: From baseline up to 7 days

    As measured by Platelet Function Analyzer (PFA) 100/200

Sponsors and collaborators

Lead sponsor

Ferring Pharmaceuticals

Industry

Registry information

Official study title

Documentation of the Efficacy of Desmopressin (MINIRIN Parenteral 4 Microgram/ml Solution for Injection) Within the Context of Surgical Procedures

Acronym: RAPID

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Feb 23, 2015
Registry last updated
Jun 2, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.