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NCT07362901

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

Not yet recruiting Last updated 23 January 2026
What this trial tests

trial testing postoperative precise education in Aortic Dissection Aneurysm in 132 participants. Not yet recruiting.

Timeline
1 January 2026
Primary endpoint
1 June 2027
1 December 2028

Quick facts

Lead sponsorFirst Affiliated Hospital of Zhejiang University
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment132
Start date1 January 2026
Primary completion1 June 2027
Estimated completion1 December 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

First Affiliated Hospital of Zhejiang University

Who can join

Eligibility, any sex, with Aortic Dissection Aneurysm or Aortic Dissection Rupture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Aortic Dissection Aneurysm

Currently open trials in the same condition.

Other First Affiliated Hospital of Zhejiang University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07362901.

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