Not Yet RecruitingNot Applicable

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

China120 participantsStarted 2026-01-01

Plain-language summary

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.

Who can participate

SexALL

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Inclusion criteria

✓. Diagnosed with thoracoabdominal aortic disease
✓. Patients who underwent endovascular treatment of the thoracoabdominal aorta via the femoral artery approach

Exclusion criteria

✕. 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.)
✕. Patients who have undergone endovascular aortic treatment via femoral artery access prior to this procedure due to other diseases (not related to the current aortic disease)

What they're measuring

The incidence of postoperative discomfort symptoms

Timeframe: 6, 24, and 48 hours postoperatively

Trial details

NCT IDNCT07114185

SponsorFirst Affiliated Hospital of Zhejiang University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-12-01

Contact for this trial

xiaoya zhang

+8613516729415 2470575102@qq.com

View on ClinicalTrials.gov More Aortic Aneurysm and Dissection trials