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Association of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers With Post-Stroke Pneumonia: A Real-World Retrospective Cohort Study

T

Tianjin University of Traditional Chinese Medicine

Status

Not yet enrolling

Conditions

Post-stroke Pneumonia

Treatments

Drug: Calcium Channel Blockers
Drug: angiotensin converting enzyme inhibitors
Drug: Angiotensin Receptor Blockers

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this retrospective cohort study is to determine if Angiotensin-Converting Enzyme Inhibitors (ACEIs) and Angiotensin Receptor Blockers (ARBs) can lower the risk of post-stroke pneumonia. With an active comparator, new-user design, we selected new users of Calcium Channel Blockers (CCBs) as the reference group to compare against new users of ACEIs/ARBs.

Enrollment

13,656 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosis of both stroke and hypertension, with the initial diagnosis dates for both conditions falling within the period from January 1, 2016, to December 31, 2024.Definition of Stroke: International Classification of Diseases, 10th Revision (ICD-10) codes I60-I64, or a primary diagnosis of stroke-related conditions in inpatient/outpatient medical records, including but not limited to: cerebral hemorrhage, hemorrhagic stroke, cerebral infarction, ischemic stroke, cerebral ischemia, brainstem infarction.Definition of Hypertension: ICD-10 code I10, or inpatient/outpatient medical records containing diagnostic names such as hypertension, benign hypertension, hypertensive crisis.
  2. At least one prescription filled from any of the five major classes of antihypertensive medications: Angiotensin-Converting Enzyme Inhibitors (ACEI), Angiotensin II Receptor Blockers (ARB), Beta-blockers, Calcium Channel Blockers (CCB), or Diuretics. Furthermore, there must be no record of any ACEI, ARB, or CCB prescriptions within the 12 months immediately preceding the first ACEI, ARB, or CCB prescription.
  3. Aage ≥18 years.

Exclusion criteria

  1. Data anomalies or errors(such as an inaccurately recorded date of death).
  2. Concurrent use of two or three drug classes among ACEI, ARB, and CCB at any time.
  3. Any recorded diagnosis of pneumonia prior to the initiation of the first antihypertensive medication.Definition of Pneumonia: ICD-10 codes J12-J18 or J69, or inpatient/outpatient medical records containing diagnostic names such as pulmonary infection, pneumonia, lung infection.

Trial design

13,656 participants in 4 patient groups

ACEI-exposed group
Description:
Newly Initiated ACEI
Treatment:
Drug: angiotensin converting enzyme inhibitors
ARB-exposed group
Description:
Newly Initiated ARB
Treatment:
Drug: Angiotensin Receptor Blockers
CCB-exposed group1
Description:
Newly Initiated CCB
Treatment:
Drug: Calcium Channel Blockers
CCB-exposed group2
Description:
Newly Initiated CCB
Treatment:
Drug: Calcium Channel Blockers

Trial contacts and locations

0

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Central trial contact

Xiaonong Fan

Data sourced from clinicaltrials.gov

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