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

NCT02368730 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 23

Last updated 2017-06-02

No results posted yet for this study

Summary

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.

Conditions

  • Platelet Dysfunction

Interventions

DRUG

desmopressin

Sponsors & Collaborators

  • Ferring Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Clinical Development Support · Ferring Pharmaceuticals

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2016-06-30
Completion
2016-07-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02368730 on ClinicalTrials.gov