Effective Treatments for Thoracic Aortic Aneurysms (ETTAA Study): A Prospective Cohort Study

Sponsor
Papworth Hospital NHS Foundation Trust (Other)
Overall Status
Unknown status
CT.gov ID
NCT02010892
Collaborator
(none)
2,200
1
64.9
33.9

Study Details

Study Description

Brief Summary

This is a prospective observational cohort study that will collect data from the point of referral through to secondary care, aiming for 3 years median follow-up (range 1-5 years). The data collected will allow estimation of the success of any intervention (in terms of reducing rate of aneurysm growth, rupture or dissection) as well as estimation of the risks associated with the three procedures. Clinical outcomes in the three treatment groups will be described.

Aims

We aim to answer the following questions:
  1. Without procedural intervention for chronic thoracic aortic aneurysm (CTAA), what is the risk of aneurysm growth, dissection, rupture, permanent neurological injury or death? What is the effect on quality of life (QoL)?

  2. If a patient has endovascular stent grafting (ESG) or open surgical repair (OSR), what is the risk of growth, dissection, rupture, permanent neurological injury or death?

  3. How does QoL change from pre- to post intervention?

  4. Can aneurysm or patient related predictors of good/poor treatment outcomes be determined?

  5. What is the most cost-effective strategy in:

  6. Patients eligible for either ESG or OSR?

  7. Patients eligible for either ESG or best medical therapy (BMT)?

  8. Patients eligible for either watchful waiting (WW) or intervention (ESG/ OSR)?

  9. What further research is required? What would be the most important research to pursue?

Condition or Disease Intervention/Treatment Phase
  • Procedure: Stent Grafting (ESR)
  • Procedure: Open Surgery (OSR)

Study Design

Study Type:
Observational
Anticipated Enrollment :
2200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Effective Treatments for Thoracic Aortic Aneurysms (ETTAA Study): A Prospective Cohort Study
Study Start Date :
Feb 1, 2014
Anticipated Primary Completion Date :
Jan 1, 2019
Anticipated Study Completion Date :
Jul 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Watchful Waiting

Patients with aneurysms considered to be at low risk of rupture will remain under surveillance with annual CT / MRI scans and multi-disciplinary team review (as per local practice). These patients' data will contribute to the natural history component of the study.

Best Medical Therapy

This refers to lifestyle modification (smoking cessation and dietary management) as well as medical management of hypercholesterolaemia and hypertension for patients who are considered unsuitable for, or who refuse, OSR / ESG.

Open Surgery (OSR)

Replacement of the aneurysmal aorta with prosthetic conduit via a sternotomy or thoracotomy with circulatory support.

Procedure: Open Surgery (OSR)

Stenting (ESR)

Endovascular repair of the aneurysm via transluminal introduction of a stent-graft under X-ray guidance. Hybrid procedures that comprise a combination of a conventional surgical component and a transluminal repair are to be included in this group.

Procedure: Stent Grafting (ESR)

Outcome Measures

Primary Outcome Measures

  1. Aneurysm Growth [1, 2, 3 , 4 and 5 years post recruitment]

  2. Quality of life [1, 2, 3 , 4 and 5 years post recruitment]

  3. Freedom from reintervention [1, 2, 3 , 4 and 5 years post recruitment]

  4. Freedom from death or permanent neurological injury [1, 2, 3 , 4 and 5 years post recruitment]

  5. Costs to the NHS [1, 2, 3 , 4 and 5 years post recruitment]

  6. Incremental cost per quality adjusted life year gained [1, 2, 3 , 4 and 5 years post recruitment]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Thoracic Aortic Aneurysm > 4cm

  • Age ≥18 years

  • Able to give informed consent

Exclusion Criteria:
  • Intervention required below the level of the coeliac axis

  • Acute dissection or malperfusion syndromes (such as myocardial infarction,acute stroke or limb ischaemia)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Papworth Hospital Cambridge Cambs United Kingdom CB23 3RE

Sponsors and Collaborators

  • Papworth Hospital NHS Foundation Trust

Investigators

  • Study Chair: Stephen Large, FRCS, Papworth Hospital NHS Foundation Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Papworth Hospital NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT02010892
Other Study ID Numbers:
  • P01633
  • 11/147/03
First Posted:
Dec 13, 2013
Last Update Posted:
May 6, 2016
Last Verified:
May 1, 2016
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2016