Actively Recruiting

Age: 18Years +
All Genders
ID05342233

Comparison of Conservative and Endovascular Treatment for Spontaneously Isolated Superior Mesenteric Artery Dissection: A Real-world, Multicenter, Observational Study

Led by Xiangya Hospital of Central South University · Updated on 2022-04-22

200

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

X

Xiangya Hospital of Central South University

Lead Sponsor

T

The First Medical Center of Chinese PLA General Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying Spontaneous Isolated Superior Mesenteric Artery Dissection (SISMAD), a condition increasingly diagnosed but with limited evidence guiding treatment. This observational study compares the effects of conservative treatment versus endovascular treatment to understand which approach better helps patients with this condition. The study is sponsored by Xiangya Hospital of Central South University and aims to provide real-world evidence to improve clinical decisions for SISMAD. Participants receive either endovascular treatments or conservative care. Conservative treatment includes managing blood pressure, bowel rest, antithrombotic therapy, nutritional support, and pain control. The study observes these treatment groups over time to assess outcomes without altering usual care. There is no randomization or blinding since this is an observational study. Participants will be followed for up to five years with regular monitoring of symptom relief and survival. Researchers will also track reintervention needs, recurrence, disease complications, and artery remodeling. Patients will undergo clinical evaluations and imaging to assess their condition's progress. The study involves long-term observation to gather comprehensive data on treatment effects and safety.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 and above
  • Diagnosed with isolated superior mesenteric artery dissection confirmed by CTA with clear symptoms or history
  • Signed informed consent and willing to receive treatments
Not Eligible

You will not qualify if you...

  • Severe symptoms requiring exploratory laparotomy
  • Having aortic dissection, iliac artery dissection, or autoimmune vasculitis
  • Mental illness preventing cooperation
  • Allergy to contrast agents or contraindications to conservative treatment drugs
  • Pregnancy, breastfeeding, or recent plans to give birth
  • Participation in other clinical trials
  • Deemed unsuitable for participation by investigators

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 5 years

Participants who undergo routine care for isolated superior mesenteric artery dissection are observed to compare outcomes between conservative and endovascular treatments.

Regular visits as per routine clinical care up to 5 years

Trial Site Locations

Total: 1 location

1

Xiangya Hospital of Central South University

Changsha, Hunan, China

Actively Recruiting

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Research Team

W

Wang WEI, Ph.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Frequently Asked Questions

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