Distinguished in Pulmonary Hypertension

Dr. Robert G. Weiss

Cardiology
Johns Hopkins University
601 N Caroline St, 
Baltimore, MD 
Clinical Trials:Currently Recruiting for 1 Trial
Accepting New Patients
Distinguished in Pulmonary Hypertension
Johns Hopkins University
601 N Caroline St, 
Baltimore, MD 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Robert Weiss is a Cardiologist in Baltimore, Maryland. Dr. Weiss is rated as a Distinguished provider by MediFind in the treatment of Pulmonary Hypertension. His top areas of expertise are Pulmonary Hypertension, Heart Attack, Pulmonary Veno-Occlusive Disease, Heart Failure with Preserved Ejection Fraction (HFpEF), and Cardiac Ablation. Dr. Weiss is currently accepting new patients.

His clinical research consists of co-authoring 131 peer reviewed articles and participating in 8 clinical trials. MediFind looks at clinical research from the past 15 years.

Specialties
Cardiology
Licenses
Internal Medicine in MD
Hospital Affiliations
The Johns Hopkins Hospital
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO

Locations

JOHNS HOPKINS UNIVERSITY
601 N Caroline St, Baltimore, MD 21287
Other Locations
JOHNS HOPKINS UNIVERSITY
600 N Wolfe St, Blalock 266, Baltimore, MD 21287
JOHNS HOPKINS UNIVERSITY
4940 Eastern Ave, Baltimore, MD 21224
JOHNS HOPKINS UNIVERSITY
10803 Falls Rd, Lutherville, MD 21093

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

8 Clinical Trials

Functional Energetics and Imaging for Phenotypic Characterization of Patients at Risk for Sudden Cardiac Death
Functional Energetics and Imaging for Phenotypic Characterization of Patients at Risk for Sudden Cardiac Death
Enrollment Status: Recruiting
Publish Date: January 10, 2025
A Pivotal USA Randomized, Evaluator-blinded, Active-controlled, Multi-center, Split-face Comparison Study of Emervel® Deep Lidocaine Versus Juvederm® Ultra Plus in the Treatment of Moderate to Severe Facial Wrinkles and Folds
A Pivotal USA Randomized, Evaluator-blinded, Active-controlled, Multi-center, Split-face Comparison Study of Emervel® Deep Lidocaine Versus Juvederm® Ultra Plus in the Treatment of Moderate to Severe Facial Wrinkles and Folds
Enrollment Status: Completed
Publish Date: October 23, 2023
Intervention Type: Device
Study Phase: Not Applicable
A Phase 3, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of Cortexolone 17α-Propionate (CB-03-01) Cream, 1% Applied Twice Daily for 12 Weeks in Subjects With Facial Acne Vulgaris
A Phase 3, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of Cortexolone 17α-Propionate (CB-03-01) Cream, 1% Applied Twice Daily for 12 Weeks in Subjects With Facial Acne Vulgaris
Enrollment Status: Completed
Publish Date: November 20, 2020
Intervention Type: Drug
Study Phase: Phase 3
A Randomized, Double-blind, Dose-ranging Trial of Subcutaneous Sodium Deoxycholate Injections With or Without Low Dose Triamcinolone and Low Dose Lidocaine for Reduction of Submental Fat With Reduction of Pain and Swelling
A Randomized, Double-blind, Dose-ranging Trial of Subcutaneous Sodium Deoxycholate Injections With or Without Low Dose Triamcinolone and Low Dose Lidocaine for Reduction of Submental Fat With Reduction of Pain and Swelling
Enrollment Status: Completed
Publish Date: May 09, 2019
Intervention Type: Drug, Combination product
Study Phase: Phase 4
Follow-up of Patients Treated in VeClose Study (Five Years)
Follow-up of Patients Treated in VeClose Study (Five Years)
Enrollment Status: Completed
Publish Date: April 12, 2019
Intervention Type: Device
Evaluation of the Lutronic LaseMD System for the Treatment of Benign Pigmented Lesions
Evaluation of the Lutronic LaseMD System for the Treatment of Benign Pigmented Lesions
Enrollment Status: Completed
Publish Date: March 13, 2019
Intervention Type: Device
Study Phase: Not Applicable
Evaluation of VeinViewer in Cosmetic Dermatology
Evaluation of VeinViewer in Cosmetic Dermatology
Enrollment Status: Completed
Publish Date: October 17, 2018
Intervention Type: Device
Study Phase: Not Applicable
Randomized Evaluation of Heart Failure With Preserved Ejection Fraction (HFpEF) Patients With Acute Heart Failure and Dopamine (ROPA-DOP) Trial
Randomized Evaluation of Heart Failure With Preserved Ejection Fraction (HFpEF) Patients With Acute Heart Failure and Dopamine (ROPA-DOP) Trial
Enrollment Status: Completed
Publish Date: August 16, 2018
Intervention Type: Drug
Study Phase: Phase 4
View 7 Less Clinical Trials

131 Total Publications

Skeletal Muscle Quantity Versus Quality in Heart Failure: Exercise Intolerance and Outcomes in Older Patients With HFpEF Are Related to Abnormal Skeletal Muscle Metabolism Rather Than Age-Related Skeletal Muscle Loss.
Skeletal Muscle Quantity Versus Quality in Heart Failure: Exercise Intolerance and Outcomes in Older Patients With HFpEF Are Related to Abnormal Skeletal Muscle Metabolism Rather Than Age-Related Skeletal Muscle Loss.
Journal: Circulation. Heart failure
Published: June 19, 2025
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Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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