About this trial

This prospective, multicenter, open-label clinical trial is designed to evaluate the safety and efficacy of rapamycin in the treatment of communicating hydrocephalus secondary to intraventricular hemorrhage. Additionally, the underlying pathogenic mechanisms associated with this particular type of hydrocephalus will be investigated in greater depth, and populations that may benefit from rapamycin therapy will be identified.

Eligibility criteria

Qualifiers

Patients with ventricular dilatation due to intraventricular hemorrhage who clinically present with any one or more of new gait disturbances, cognitive deficits, and urinary incontinence after remission of intraventricular hemorrhage symptoms, and whose brain imaging shows an Evans index (EI) of ≥0.3

Age ≥ 18 years and ≤ 70 years

Signed informed consent form

Disqualifiers

Participation in another medical trial

Have other disease that may affect the patient's symptoms (including gait disturbance, cognitive impairment, urinary incontinence)

Allergy to the investigational drug

Reduced liver function (increased INR or alanine transaminase concentrations in plasma elevated more than 1.5 times reference values)

Trial design

Treatments tested in this trial

  • Rapamycin

Treatment groups

53 Participants
are divided into 1 treatment group

Locations

1
Beijing Tiantan Hospital, Capital Medical University100070, BeijingBeijing Municipality, China

Sponsors and collaborators

Beijing Tiantan Hospital

Lead sponsor