Healthy Clinical Trial - Timed Aspirin Chronobiome Study

Status Not yet recruiting

Clinical Trial Summary

To determine whether timed administration of aspirin ameliorates the effects of celecoxib on blood pressure.

Clinical Trial Description

Non-steroidal anti-inflammatory drugs (NSAIDs) are a commonly used and effective treatment of inflammatory pain. However, all NSAID have the potential to raise blood pressure (BP), cause the development of new hypertension or exacerbate preexisting hypertension. Strategies to mitigating that risk short of withholding the analgesic are missing. In this proposal, the investigators wish to determine whether timed administration of low dose aspirin can be developed as a low cost intervention with well-defined risk profile to mitigate the blood pressure raise associated with the COX-2 selective NSAID celecoxib. Low dose aspirin administered in the evening, but not in the morning, normalizes the mean arterial BP in clinical studies of prehypertension, mild essential hypertension and preeclampsia. The investigators will address this in an interventional study in healthy volunteers who displayed a blood pressure increase during celecoxib treatment in an ongoing study. Since individuals have varying chronotypes and work/social rhythms, parameter measuring day/night patterns, the chronobiome, will be part of this study. ;

Study Design

Related Conditions & MeSH terms

Healthy

Clinical Trial Details

NCT number	NCT03590821
Study type	Interventional
Source	University of Pennsylvania
Contact	LaVenia Banas, CRN
Phone	215-573-1862
Email	banas@pennmedicine.upenn.edu
Status	Not yet recruiting
Phase	Early Phase 1
Start date	December 2024
Completion date	May 2028

View Details

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