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An Evaluation of Patient Reported Outcomes and Clinical Outcomes

Post-Operative Complications in Cardiac Surgery

This extension study is being conducted to assess the following objectives through 12 months post-cardiac surgery:

* Patient reported outcomes (PRO), using the EQ-5D questionnaire
* Clinical outcomes

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Subjects must have completed the REN-007 study to be eligible to participate in the Extension Study.

Exclusion Criteria:

* Subjects who did not complete the REN-007 study are not eligible to participate in the Extension Study.
* Female subjects who become pregnant during the REN-007 study are not eligible to participate in the Extension Study.

Study Location

Research Site
Research Site
Kelowna, British Columbia
Canada

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Research Site
Research Site
Kingston, Ontario
Canada

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Research Site
Research Site
Montréal, Quebec
Canada

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Research Site
Research Site
Hamilton, Ontario
Canada

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Research Site
Research Site
Montréal, Quebec
Canada

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Research Site
Research Site
Saint John, New Brunswick
Canada

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Research Site
Research Site
Montréal, Quebec
Canada

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Research Site
Research Site
Québec, Quebec
Canada

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Research Site
Research Site
Saint John's, Newfoundland and Labrador
Canada

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Research Site
Research Site
Montréal, Quebec
Canada

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Study Sponsored By
Renibus Therapeutics, Inc.
Participants Required
More Information
Study ID: NCT06092970