drugset / Trial / NCT05689827

Safety and Efficacy of the Therapy With BRAINMAX® for the Treatment of Patients With Asthenia After COVID-19

NCT05689827

Phase 4 Completed 160 enrolled Promomed, LLC
RandomizedSequentialSingle-blindTreatment

Summary

This is prospective multicentre comparative randomized double blind placebo controlled study conducted in 6 medical facilities.The objective of the study is to assess the safety and efficacy of the sequential therapy with BRAINMAX®, solution for intravenous infusion and intramuscular injection, and BRAINMAX®, capsules for the treatment of patients with asthenia after having the novel coronavirus infection (COVID-19)

Timeline

Start
2022-04-05
Primary completion
2022-11-10
Completion
2022-11-10

Drugs

EvaluationDrugModalityDoseRoute
Subject EMOXYPINE Small molecule 500 mg Intramuscular
Subject Meldonium Small molecule 500 mg Intramuscular

Indications