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Effects of Precise Education on Postoperative Discomfort Symptoms in Patients With Aortic Disease Undergoing Endovascular Intervention: a Single-center Randomized Controlled Study

China132 participantsStarted 2026-01-01

Plain-language summary

The incidence and severity of post-procedural discomfort were evaluated in patients undergoing endovascular repair for aortic dissection 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

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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)
✕. Patients with intracerebral hemorrhage, symptomatic stroke, myocardial infarction, or gastrointestinal bleeding within the past 6 months; patients under 18 years old; or those who refuse to participate in the study

What they're measuring

Immobilization-Related Score

Timeframe: Perioperative

Puncture Site-Related Score

Timeframe: perioperative

Medical Adhesive-Related Skin Injury (MARSI) Score

Timeframe: perioperative

Aortic Disease-Related Score

Timeframe: perioperative

Self-Care Ability-Related Score

Timeframe: perioperative

Psychosomatic Stress-Related Score

Timeframe: perioperative

Trial details

NCT IDNCT07362901

SponsorFirst Affiliated Hospital of Zhejiang University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-06-01

Contact for this trial

Peier Shen

+8613588040680 405496770@qq.com

View on ClinicalTrials.gov More Aortic Dissection Aneurysm trials

Plain-language summary

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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)
✕. Patients with intracerebral hemorrhage, symptomatic stroke, myocardial infarction, or gastrointestinal bleeding within the past 6 months; patients under 18 years old; or those who refuse to participate in the study

What they're measuring

Immobilization-Related Score

Timeframe: Perioperative

Puncture Site-Related Score

Timeframe: perioperative

Medical Adhesive-Related Skin Injury (MARSI) Score

Timeframe: perioperative

Aortic Disease-Related Score

Timeframe: perioperative

Self-Care Ability-Related Score

Timeframe: perioperative

Psychosomatic Stress-Related Score

Timeframe: perioperative