Phase II Clinical Trial of Estradiol to Reduce Severity of COVID19 Infection in COVID19+ and Presumptive COVID19+ Patients
Trial Snapshot
- Phase
- Phase 2
- Status
- Terminated
- Sponsor
- Enrollment
- 2
- Locations
- 1
- Primary Endpoint
- Rate of Hospitalization
Study Overview
Brief Summary
The purpose of this study is to find out if estrogen, a female sex hormone, given as a patch placed on skin of COVID19 positive or presumptive positive patients for 7 days can reduce the severity of COVID19 symptoms compared to regular care.
This study has two study groups. One group will receive the study drug, a single-use Climara 25cm2 estrogen patch. The other group will receive standard of care.
Participants will be asked questions about their symptoms for up 6 times in up to 45 days.
Detailed Description
As the COVID19 pandemic has spread, it has been observed that adult men of all ages and older women are at higher risk of developing serious complications from infection with the virus. Animal model studies of SARS suggest that the age and sex difference in COVID19 symptom severity may be due to protective and acute actions of the female sex hormone estrogen. Animal and human studies support immune modulating effects of estrogen that are acute acting in viral infections and wound repair processes that may reduce the damaging effects of the virus on the lung and symptom severity.
Our hypothesis is that a short 7 day course of estradiol delivered in a transdermal patch applied to the upper buttock in COVID19+ or presumptive positive patients will be safe and will reduce symptom severity in adult men and older women when given prior to intubation. COVID19+ and presumptive positive patients not requiring intubation will be enrolled to the study and randomized to receive an estrogen patch or standard of care. Patients will be followed up at day 1, 7, 14 and 28 for clinical symptoms and disease outcomes.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Male ≥ 18 years of age or female ≥ 55 years of age
- •Documentation of COVID19 positivity or the presence of one or more of the following new onset (<7 days) clinical features defining presumptive COVID19
- •fever of >100.5°F or 38°C
- •shortness of breath
- •radiologic evidence of pneumonia
- •Able to provide informed consent
- •Able to be contacted by telephone for follow-up
Exclusion Criteria
- •Currently receiving estrogen based hormonal therapy
- •Abnormal genital bleeding
- •Protein C or Protein S deficiency
- •Pre-existing liver impairment (e.g. Hepatitis C, cirrhosis)
- •History of anaphylactic reaction or angioedema with Climara
- •Receiving lamotrigine therapy
- •Subjects with known past diagnosis of estrogen receptor positive breast cancer or endometrial cancer
- •Subjects with severe hypoxia at risk for acute intubation in ED
- •History of stroke
- •Any history of thromboembolic event including deep vein thrombosis or pulmonary emboli
- •Current use of St. John's Wort
- •Males on testosterone
- •History of myocardial infarction, cardiac stents, or active angina
Arms & Interventions
Active
Estradiol Patch
Intervention: Estradiol patch (Drug)
Outcomes
Primary Outcomes
Rate of Hospitalization
Time Frame: 30 days
Admission to hospital due to COVID-19 symptoms
Rate of Transfer to Intensive Care Unit
Time Frame: 30 days
Occurrence of admission to ICU due to COVID-19 symptoms
Rate of Intubation
Time Frame: 30 days
Occurrence of intubation
Rate of Death
Time Frame: 30 days
Occurrence of death from COVID-19
Secondary Outcomes
No secondary outcomes reported
Investigators
Sharon Nachman
Director of Pediatric Infectious Diseases
Stony Brook University