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Comparison of Conservative and Endovascular Treatment for Spontaneously Isolated Superior Mesenteric Artery Dissection

C

Central South University

Status

Enrolling

Conditions

Spontaneous Isolated Superior Mesenteric Artery Dissection

Study type

Observational

Funder types

Other

Identifiers

NCT05342233
ISMAD2022

Details and patient eligibility

About

Spontaneous isolated superior mesenteric artery dissection(SISMAD) is an increasingly diagnosed disease. However, prospective, multicenter studies that can provide evidence to support clinical decisions are very limited. This study aims to compare the therapeutic efficacy of conservative and endovascular treatment for SISMAD.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Aged 18 and above;
  2. Isolated superior mesenteric artery dissection with clear symptoms or history and confirmed by CTA
  3. Signed informed consent forms, willing to receive treatments

Exclusion criteria

  1. Symptoms are severe and patients need exploratory laparotomy;
  2. Patients with aortic dissection, iliac artery dissection, or autoimmune vasculitis;
  3. Patients with mental illness cannot cooperate subjectively;
  4. Patients who are allergic to contrast agents, or contraindicated to conservative treatment drugs, and cannot be treated with drugs;
  5. Pregnancy and breastfeeding women, or patients who have recent birth plans;
  6. Patients who are participating in other clinical projects;
  7. Patients are not suitable to participate in this study.

Trial design

200 participants in 2 patient groups

Endovascular treatment Group
Description:
Patients receiving endovascular treatments
Conservative treatment Group
Description:
Patients receiving conservative treatments, including blood pressure control, bowel rest, antithrombotic therapy, nutrition treatment and pain management.

Trial contacts and locations

1

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Central trial contact

Wang WEI, Ph.D.

Data sourced from clinicaltrials.gov

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