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AneurysmNCT02372214

Production of a Patient-specific Simulator for Endovascular Aneurysm Repair Training

A study testing Training in people with Aneurysm, run by University of Sao Paulo General Hospital at 1 site in Brazil.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to produce a patient-specific simulator for endovascular infra-renal aneurysm repair training and than analyze the effect of simulator training on the performance of vascular surgery residents. Read more about this study

Who is it for?
Any age
Conditions the study is for
Aneurysm
What is being tested?
Training
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
55 participants
Where
1 siteBrazil
Study dates
Mar 2014to Jul 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Patients with infra-renal aneurysm with diameter of 5,5cm or more
  • Residents of the last year of vascular surgery at Clinics Hospital of São Paulo University Medical School

Who cannot join

  • Patients not suitable for endovascular aneurysm repair
  • Patients with iliac aneurysm that require iliac bifurcated grafts
  • Residents who don't want participate

Trial locations and contacts

1 site in 1 country.

Brazil1 site
  • Clinics Hospital of São Paulo University Medical School

    São Paulo, São Paulo, 05403-900

Other trials in Brazil

About this study

Official title: Impact of a Patient-specific Simulation on the Learning Curve of Infra-renal Aneurysm Endovascular Repair

The purpose of this study is to produce a patient-specific simulator for endovascular infra-renal aneurysm repair training and than analyze the effect of simulator training on the performance of vascular surgery residents.

Read the detailed description

Title: Production of a patient-specific simulator for endovascular aneurysm repair training.

Clinics Hospital of São Paulo University Medical School

Introduction

The aorta aneurysm is a common clinical condition that implies in considerable threatening to the life of patients. Before the year 2000, 99% of the abdominal aortic aneurysm (AAA) repair where performed with open surgery. Nevertheless, Catheter-based minimally invasive interventions are rapidly becoming the preferred initial treatment in patients with vascular disease . After 2004, the endovascular treatment of AAA increased to 52%. This changing venue requires a shift in our approach to training both fellows as well as general surgical residents during their exposure to vascular surgery.

Currently, supervised training with progressive exposure to procedures is the norm. Nevertheless, simulations based training may allow a shortening of the learning curve and avoid the exposure of the patients to unnecessary risks.

Using the rapid prototyping it is possible to build models in flexible materials that are helpful for training surgeons while simulating surgical procedures in a very realistic manner.

The possibility of training surgical procedures in general as well as patient-specific procedures might improve the surgeon's abilities and results . Rapid prototyping models allow for intensive training of young surgeons, e.g., for endovascular stent implantation simulating in vivo conditions and real tissues without any risk of patient complications and with no exposure of the surgeon to radiation or biologic risks.

After being adequately trained on models, surgeons feel more confident while going to the operating room for actual surgery. Besides, the pre-operative simulation of a specific and complex surgery provides a unique opportunity to employ surgical steps in order to determine the best operating strategy.

Simulators for catheter-based intervention have been available for approximately 5 years, and the technology is evolving rapidly. Currently, simulators are expensive and access has been limited. The ultimate test of simulation is to demonstrate that performance improves in the operating room.

To this end, we designed a randomized prospective study to describe the creation of a patient-specific simulator for training in endovascular infra-renal aneurysm correction and we will analyze the effect of simulator training on the performance of vascular surgery residents.

Objectives:

Primary: Production of a patient-specific simulator for training in endovascular infra-renal aneurysm repair.

Secondary: Analyze the effect of simulator training on the performance of vascular surgery residents.

Methods:

Production of a patient-specific simulator: The process chain on the production of a three-dimensional rapid prototype model consists of the following three steps: Image acquisition, Image post-processing and 3D printing. Patients will undergo a angioCT, with slice thickness of 1mm. Acquired data will be saved in the common DICOM format (Digital Imaging and Communications in Medicine). Dedicated high performance workstations equipped with post-processing tools will be used for processing the DICOM images generated during acquisition. The DICOM data will be transformed into a STL (Surface Tesselation Language) file format. The 3D machine reads in data from a CAD drawing and lays down successive layers of liquid, powder, or the sheet material, and in this way builds up the model from a series of cross sections. With that, a patient-specific pulsatile model will be produced.

Analyze the effect of simulator training on the performance of vascular surgery residents: The study will be performed during a period of two years (2014 and 2015), at the Clinics Hospital of São Paulo University Medical School.

All the endovascular aneurysm repair (EVAR) performed in during this time will be analyzed. According to the average number of EVAR in this service, we calculate that this research will include at least 60 patients.

Ten vascular surgery residents coursing the last year of practice will be randomized into the 2 groups (this is the total number of residents in our service).

Inclusion Criteria:

  • Patients with infra-renal aneurysm with diameter of 5,5cm or more
  • Residents of the last year of vascular surgery at Clinics Hospital of São Paulo University Medical School

Exclusion Criteria:

  • Patients not suitable for endovascular aneurysm repair
  • Patients with iliac aneurysm that require iliac bifurcated grafts
  • Residents who don't want participate
  • Group 1 (30 patients/5residents): patients will undergo endovascular aneurysm repair according to the hospital routine. The residents will perform the procedure under supervision of a senior surgeon. It is an observational part of the study, which has already been done during the year 2014.
  • Group 2 (30 patients/5residents): patients will have their aneurysm impressed by a 3D printing. The senior vascular surgeon and the residents of this group will be able to practice the procedure in the model as many times as they wish before the surgery. After the training, the EVAR will be performed according to the routine of the hospital.

During the surgery, objective parameters will be analyzed: radioscopy time, volume of contrast injected, total procedure time, number of catheters and guide-wires used, technical success. The patients will be followed until they leave the hospital. Morbidity (myocardial infarction, renal failure, pulmonary complications) and mortality during the peri-operative time (30 days) will be analyzed. The surgeon will answer a questionnaire about the experience. The data from the two groups will be compared.

This study is approved by the national ethics committee.

Conditions
Aneurysm
Being tested
Training
Keywords
Endovascular Procedures, 3D printing, Simulation, Training, Learning curve, Education
Medical subject headings
Aneurysm

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TrainingProcedure or surgery

    Patients will have their aneurysm impressed by a 3D printing. The senior vascular surgeon and the residents of this group will be able to practice the procedure in the model as many times as they wish before the surgery. After the training, the EVAR will be performed according to the routine of the hospital.

Study groups in NCT02372214
Study groupRoleWhat they receive
Group 1No intervention30 patients/5 vascular surgery residents The residents of the last year of vascular surgery will perform the procedure under supervision of a senior surgeon
Group 2Experimental30 patients/5 vascular surgery residents Patients will have their aneurysm impressed by a 3D printing. The senior vascular surgeon and the residents of this group will be able to practice the procedure in the model as many times as they wish before the surgery. After the training, the EVAR will be performed according to the routine of the hospital.
Receives: Procedure: Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Fluoroscopy time

    The total fluoroscopy time in every surgery will be counted, measured in minutes

    Measured: 2 years - all the surgeries

Secondary outcomes (6)
  1. Number of participants with Myocardial infarction.

    The Number of participants with Myocardial infarction (CKMB or Troponin positive curve or change in ECG) within 30 days of the surgery.

    Measured: 30 days

  2. Number of participants with Renal disfunction

    Number of participants with renal disfunction (necessity of hemodialysis or enhance of creatinine level) within 30 days of the surgery.

    Measured: 30 days

  3. Death

    Measured: 30 days

  4. Number of participants with Pulmonary complications

    Number of participants with Pulmonary complications (Pneumonia, Pulmonary congestion) within 30 days of the surgery.

    Measured: 30 days

  5. Technical success (Endoprosthesis located in the right position, no endoleak type 1)

    Endoprosthesis located in the right position, no endoleak type 1

    Measured: 30 days

  6. Contrast volume in each surgery

    The volume of contrast used in all the surgeries will be measured in milliliters during the period of the study.

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Feb 2015 (estimated)
  2. Study startMar 2014
  3. Primary completionMar 2016
  4. Study completionJul 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
55 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02372214
Sponsor's protocol ID
3Daneurysm
Status last verified
Jul 2016
First submitted
2 Feb 2015
Last updated
8 May 2018
Results posted
No
Data monitoring committee
Yes
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Training in people with Aneurysm, run by University of Sao Paulo General Hospital at 1 site in Brazil.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 May 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Fluoroscopy time (time frame: 2 years - all the surgeries). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 May 2018.

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