A Prospective Study of Discomfort Symptoms in Patients With Aortic Disease After Endovascular Intervention

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorFirst Affiliated Hospital of Zhejiang University

About this trial

The incidence and severity of post-procedural discomfort were evaluated in patients undergoing endovascular repair for aortic disease across six symptom-related dimensions: immobilization-related issues, puncture site discomfort, adhesive-induced skin reactions, post-stent implantation syndrome, impairment in self-care ability, and physical/psychological stress responses.

Eligibility criteria

Qualifiers

Diagnosed with thoracoabdominal aortic disease

Patients who underwent endovascular treatment of the thoracoabdominal aorta via the femoral artery approach

Disqualifiers

Aortic disease caused by infection

Aortic disease caused by trauma

Aortic disease treated by open abdominal surgery

Presence of systemic diseases uncontrollable by current medical standards (e.g., severe cardiac, pulmonary or hepatic dysfunction; advanced malignancy; cachexia; refractory severe coronary artery disease symptoms; coagulation disorders caused by genetic diseases, etc.)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

120 Participants
are grouped into 1 trial group