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A pilot study assessing the effectiveness of oral Propranolol in preventing epistasis in patients with Hereditary Haemorrhagic Telangiectasia.

A pilot study assessing the effectiveness of oral Propranolol in preventing epistasis in patients with Hereditary Haemorrhagic Telangiectasia.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001020178
Acronym
ProHHT
Enrollment
14
Registered
2019-07-16
Start date
2019-09-04
Completion date
2020-02-25
Last updated
2026-08-24

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

Conditions

None listed

Brief summary

This study will review the intervention of administration of oral propranolol tablets to patients with HHT (Hereditary Haemorrhagic Telangiectasia) . Patients will be monitored to see if Propranolol helps reduce epistaxis (nosebleeds) . The most common symptom of HHT is having recurrent, spontaneous nosebleeds. Propranolol has been used for a similar purpose in another group of patients with good effect. If it should work it would be a very simple and cost effective way to reduce patient symptoms and approve quality of life for these patients..

Interventions

The medication Propranolol oral tablets will be prescribed for the patients at a dose of 40mg once daily for 6 months. Adherence will be monitored using a 'drug dispensation and accountability log". This will record exactly what is dispensed to the patient and on return of the propranolol bottle it will be recorded how many tablets were actually taken by the patient to measure compliance.

Sponsors

Royal brisbane and Women's Hospital
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Participants with a diagnosis of HHT according to curacao criteria score of >4 Participants with an Epistaxis severity score of >4 despite conventional treatment

Exclusion criteria

Absolute contraindication to Propranolol e.g. Bradycardia Pregnancy or breast feeding Planned surgical intervention for epistaxis control Deemed by cardiologist as unsuitable for taking Propranolol medication

Outcome results

None listed

Source: ANZCTR · Data processed: Aug 31, 2026