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Clinical Trial Summary

The purpose of this study is to assess the baseline sleep pattern disruption for patients starting oral propranolol at the standard BID dosing regimen compared to the control (timolol) group and to determine if there is a significant improvement in the sleep patterns in infants taking oral propranolol on the TID dosing regimen versus the control (timolol) group


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05479123
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact Matthew R Greives, MD
Phone 713-500-7275
Email Matthew.R.Greives@uth.tmc.edu
Status Recruiting
Phase Phase 4
Start date June 23, 2022
Completion date July 31, 2025

See also
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Recruiting NCT03237637 - Comparative Study to Evaluate the Effectiveness of Atenolol and Propranolol in the Treatment of Infantile Hemangiomas Phase 3
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Completed NCT04105517 - Hemangiol, Post Marketing Surveillance Study
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Completed NCT01056341 - Study to Demonstrate the Efficacy and Safety of Propranolol Oral Solution in Infants With Proliferating Infantile Hemangiomas Requiring Systemic Therapy Phase 2/Phase 3
Not yet recruiting NCT04684667 - ''Efficacy of Propranolol in the Treatment of Infantile Hemangioma" Phase 2
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Recruiting NCT03173352 - A Prospective Study on the Incidence and Related Risk Factors of Infantile Hemangioma in China N/A