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NCT05251974
Assay to Measure Beta Blocker Adherence
trial testing Quest beta blocker assay in Congestive Heart Failure in 27 participants. Terminated before completion.
15 November 2023
Quick facts
| Lead sponsor | Summa Health System |
|---|---|
| Status | Terminated |
| Study type | OBSERVATIONAL |
| Enrollment | 27 |
| Start date | 2 March 2022 |
| Primary completion | 15 November 2023 |
| Estimated completion | 15 November 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Quest beta blocker assay
Conditions studied
- Congestive Heart Failure — all drugs for Congestive Heart Failure →
- Medication Adherence — all drugs for Medication Adherence →
Sponsor
Summa Health System
Who can join
Adults 18 to 89, any sex, with Congestive Heart Failure or Medication Adherence. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study will assess the feasibility and efficacy of using serum assay developed by Quest Diagnostics to detect the presence of beta blockers, specifically carvedilol and metoprolol succinate, in patients with heart failure.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05251974
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Congestive Heart Failure
Currently open trials in the same condition.
- NCT07008365 — The Role of intraABDOminal Pressure and Point Of Care UltraSound to Guide Decongestive Therapy in Heart Failure · Phase 3 · recruiting
- NCT06526884 — Quasi-Randomized Evaluation of the UCLA Next Day Clinic (NDC) · NA · active not recruiting
- NCT06495892 — PVP-Guided Decongestive Therapy in HF 2 · Phase 4 · recruiting
- NCT06374277 — Pharmacy-led Transitions of Care Intervention to Improve Medication Adherence · NA · recruiting
- NCT05971225 — Verifying Remote Monitoring Effect on Net Cardiovascular Outcome; RemoteVerify (RêVe) · NA · recruiting
Other Summa Health System trials
Trials by the same sponsor.
- NCT05518877 — Low Dose Ketamine Infusion for Analgesia in the Emergency Department to Reduce Side Effects · Phase 4 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05251974 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Summa Health System
- Last refreshed: 22 November 2023
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/NCT05251974.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing