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

This trial does not accept healthy volunteers

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 population

Patients with aortic dissection undergoing endovascular treatment

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 1 trial group
Group A: 1

Trial outcomes

Primary outcomes

1

The incidence of postoperative discomfort symptoms

Based on six dimensions-immobilization-related, puncture site-related, adhesive-related skin reactions, aortic disease-related symptoms, self-care ability, and psychosomatic stress-patients were assessed at 6, 24, and 48 hours postoperatively using a structured questionnaire. The primary objective was to assess the incidence of postoperative complications and the severity of pain.

Time frame
6, 24, and 48 hours postoperatively

Secondary outcomes

Other outcomes

Sponsors and contacts

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