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Assessment of the use of spironolactone on the endothelial glycocalyx in high blood pressure

Assessment of spironolactone on the endothelial glycocalyx in hypertension

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000933459
Acronym
ASGARD
Enrollment
30
Registered
2016-07-13
Start date
2016-07-15
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The glycocalyx is a particle that is important in maintaining blood vessel health. High blood pressure is common, closely related to salt regulation, and affects the health of blood vessels. Animal studies have shown that the glycocalyx is affected in high blood pressure. Laboratory studies indicate that the use of spironolactone, a common blood pressure medication, can offset the effects of a high-salt environment on the glycocalyx. The purpose of this study is to assess if the glycocalyx is affected in people who have high blood pressure, whether the glycocalyx can be improved with good blood pressure control, and whether spironolactone has any additional protective benefits on the glycocalyx.

Interventions

Spironolactone 25mg, oral tablet, once daily. Adherence to be monitored by questionnaire and return of empty drug packets.

Sponsors

Department of Renal Medicine, Box Hill Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Hypertension on 24-hr ambulatory blood pressure monitoring (>140/90mmHg) and/or hypertensive event e.g. stroke Microalbuminuria (spot urine ACR > 3 mg/mmol)

Exclusion criteria

Malignancy, pregnancy, inability to consent, known haematological disorders, eGFR <60

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026