Uninterrupted Direct-acting Oral Anticoagulation in Patients Undergoing Transradial Percutaneous Coronary Procedures

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Up to 20-30% of patients who are candidates for direct oral anticoagulation (DOAC) present with concomitant ischemic heart disease and often require coronary angiography with or without percutaneous coronary intervention (PCI). The decision whether to continue the DOAC throughout periprocedural period or interrupt DOAC before planned procedure represents a substantial challenge in daily clinical practice. The objective of this study is to evaluate the safety of uninterrupted direct-acting oral anticoagulation in patients undergoing trans-radial percutaneous coronary procedures.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Patients under anticoagulation with DOAC and any indication for diagnostic or therapeutic trans-radial percutaneous coronary procedures. At least 25% of the population undergoing PCI will be included.

Locations
Other Locations
Italy
Humanitas Research Hospital
NOT_YET_RECRUITING
Rozzano
Spain
Hospital del Mar
RECRUITING
Barcelona
Hospital La Paz
RECRUITING
Madrid
Hospital Universitario y Politécnico La Fe
RECRUITING
Valencia
Contact Information
Primary
Jorge Sanz Sanchez, MD, PhD
sjorge4@gmx.com
440087
Time Frame
Start Date: 2022-01-20
Estimated Completion Date: 2024-04-20
Participants
Target number of participants: 200
Treatments
Experimental: Uninterruped direct-acting oral anticoagulation
Uninterrupted direct-acting oral anticoagulation in patients undergoing trans-radial percutaneous coronary procedures
Sponsors
Leads: Hospital Universitario La Fe

This content was sourced from clinicaltrials.gov