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NCT06092970

An Evaluation of Patient Reported Outcomes and Clinical Outcomes

Active, enrolled Last updated 1 August 2025
What this trial tests

trial testing RBT-1 in Post-Operative Complications in Cardiac Surgery in 379 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
16 October 2023
Primary endpoint
30 June 2026
30 June 2026

Quick facts

Lead sponsorRenibus Therapeutics, Inc.
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment379
Start date16 October 2023
Primary completion30 June 2026
Estimated completion30 June 2026
Sites39 locations across Canada, United States

Drugs / interventions tested

Conditions studied

Sponsor

Renibus Therapeutics, Inc. — full company profile →

Who can join

18 and older, any sex, with Post-Operative Complications in Cardiac Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of RBT-1

Trials testing the same drug.

Other Renibus Therapeutics, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06092970.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing