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In-Hospital Detection of Elevated Blood Pressure (INDEBP)

A

Annina Vischer

Status

Enrolling

Conditions

Blood Pressure, High
Hypertension

Treatments

Other: Postponement of antihypertensive treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT06132451
INDEBP-prospective
2023-01566 (Other Identifier)

Details and patient eligibility

About

The goal of this clinical trial is to analyse the prevalence of new or uncontrolled arterial hypertension (AHT) after hospital discharge of medical in-patients with elevated blood pressure (BP) values during hospitalisation.

The main questions it aims to answer are:

  • Do elevated BP values during hospitalisation correspond to new or uncontrolled AHT after hospital discharge?
  • Is it safe to postpone adaption of antihypertensive treatment until after proper evaluation of AHT after hospital discharge?

Participants will either be treated according to their physicians' decision or antihypertensive treatment adaptions will be postponed until after hospital discharge.

Enrollment

800 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient hospitalized on the internal medicine ward for non-cardiovascular causes, i.e. patients hospitalized for conditions, which are not acutely worsened by uncontrolled AHT
  • Asymptomatic elevated BP values (defined as 140-180 mmHg systolic and/or 90-110 mmHg diastolic) on at least 2 occasions
  • Ability to understand study procedures and to provide written informed consent

Exclusion criteria

  • Hospitalization for any conditions which can be worsened by uncontrolled AHT:
  • Cerebrovascular events
  • Acute coronary syndrome
  • Acute or decompensated heart failure
  • Any condition preventing ABPM
  • Pregnant or lactating women
  • Failure to provide informed consent

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

800 participants in 2 patient groups

Usual practice arm
No Intervention group
Description:
Patients will be treated according to their treating physicians' decision.
Postponement of treatment arm
Other group
Description:
Antihypertensive treatment adaptions will be postponed until after a 24h ambulatory blood pressure measurement (ABPM) 4 weeks after hospital discharge.
Treatment:
Other: Postponement of antihypertensive treatment

Trial contacts and locations

1

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Central trial contact

Annina Vischer, M.D.

Data sourced from clinicaltrials.gov

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