UnknownPhase 1

Oral Propanolol for Surgically Inaccessible Cavernous Malformations

United States346 participantsStarted 2018-02-07

Plain-language summary

The purpose of this study is to evaluate the role of propranolol as an alternative treatment for cavernous malformation in patients that may not be ideal candidates for surgery.

Who can participate

Age range

1 Year – 80 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Diagnosis of isolated or familial cavernous malformation syndrome:
. Written and informed consent obtained prior to study enrollment.
. Subject is able and willing to return for outpatient visits.
. Negative pregnancy test at time of enrollment for women and child-bearing potential.

Exclusion criteria

. Age less than 1 year-old.
. Propranolol allergy or allergy to other b-blockers.
. Estimated life expectancy of less than 1 year.
. History of severe anemia, cardiac dysfunction, or diabetes.
. A psychiatric or substance abuse problem that may interfere with study compliance.
. Pregnant and lactating women.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Number of symptomatic and silent hemorrhages on MRI

Timeframe: 36 months

Trial details

NCT IDNCT03523650

SponsorUniversity of Virginia

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-01

View on ClinicalTrials.gov More Cavernous Malformations,Cerebral and/or Spinal trials