Documentation of the Efficacy of Desmopressin Within the Context of Surgical Procedures (RAPID)

Ferring

Status: Completed

Conditions: Platelet Dysfunction

Treatments: Drug: desmopressin

Study type: Observational

Funder types: Industry

Identifiers

NCT02368730

000149

Details and patient eligibility

About

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.

Enrollment: 23 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

23 participants in 1 patient group

desmopressin

Description:

Treatment according to standard clinical practice.

Treatment:

Drug: desmopressin