NGS Strategy Effectiveness in Molecular Diagnosis

Sponsor
Istituto Ortopedico Rizzoli (Other)
Overall Status
Completed
CT.gov ID
NCT03557567
Collaborator
Catholic University of the Sacred Heart (Other), Regione Emilia-Romagna (Other)
400
35.1

Study Details

Study Description

Brief Summary

The coming out of Next Generation Sequencing (NGS) technologies, with documented advantages and reduced costs respect to Sanger sequencing, has provided new appealing approaches to diagnostic testing. Despite this, its use for routine diagnostic purposes requires certification in terms of reliability, as well as a cost-effectiveness evaluation.

To test the feasibility of using the Ion Torrent Personal Genome Machine (PGM) in clinical diagnosis, we assessed its performance to detect point mutations and big rearrangements previously identified with standard techniques. The diagnostic accuracy and the cost-effectiveness will be evaluated by Health Technology Assessment (HTA) analyses.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: NGS molecular screening

Study Design

Study Type:
Observational
Actual Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Other
Actual Study Start Date :
Sep 29, 2014
Actual Primary Completion Date :
Apr 1, 2017
Actual Study Completion Date :
Sep 1, 2017

Arms and Interventions

Arm Intervention/Treatment
MO patients

Diagnostic Test: NGS molecular screening

OI patients

Diagnostic Test: NGS molecular screening

Outcome Measures

Primary Outcome Measures

  1. Assessment of the accuracy of the Ion Torrent PGM platform for genetic variant detection (Diagnostic sensitivity evaluation) [at 30 months]

    The accuracy of the Ion Torrent Personal Genome (PGM) to identify disease-causing mutations in patients affected by Multiple Osteochondromas (MO) and Osteogenesis Imperfecta (OI) needs to be validated for its routine diagnostic clinical use. To asses this, we will compare results obtained with the new NGS approach with those previously obtained with standard techniques (DHPLC/Sanger + MLPA) in a number of MO and OI patients.

  2. HTA analysis to assess the cost-effectiveness, organizational and social implications of a screening strategy based on the IonPGM platform [at 36 months]

    To demonstrate the pertinence in the use of this innovative technology in health care, we will examine the medical, social and economic implications according with Health Technology Assessment (HTA), a multi-disciplinary field of policy analysis applied to many different health care technologies before their diffusion and use. HTA aims at evaluating the real effectiveness of medical interventions, their proper use, access criteria and qualitative improvements, the clinical and organizational benefits, therefore suggesting how to manage, promote and discourage them.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of Multiple Osteochondroma

  • Clinical diagnosis of Osteogenesis Imperfecta

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Istituto Ortopedico Rizzoli
  • Catholic University of the Sacred Heart
  • Regione Emilia-Romagna

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Istituto Ortopedico Rizzoli
ClinicalTrials.gov Identifier:
NCT03557567
Other Study ID Numbers:
  • PRUA1GR-2013-00000177
First Posted:
Jun 15, 2018
Last Update Posted:
Jun 18, 2018
Last Verified:
Jun 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2018