A Study to Assess the Safety and Efficacy of Centhaquine in Hypovolemic Shock Patients

Recruiting Phase 4 Interventional Study
Hypovolemic Shock
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
400 (estimated)
Sponsor
Pharmazz, Inc. · Industry
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About This Trial
This is a prospective, multi-centric, open-labeled, phase-IV clinical study to evaluate the safety and efficacy of centhaquine citrate (LYFAQUIN™), a first-in-class drug for treating hypovolemic shock, a life-threatening condition caused by severe blood or fluid loss. Centhaquine has been found to be an effective resuscitative agent in rat, rabbit, and swine models of hemorrhagic shock. It has dem…
Trial Locations
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Eligibility Criteria
Inclusion Criteria • Adult hypovolemic shock patients aged 18 years or older admitted to the emergency room or ICU with systolic blood pressure ≤ 90 mmHg at presentation and continue to receive standard shock treatment. Blood Lactate level indicative of hypovolemic shock (\>2.0 mmol/L). Exclusion …
Contacts

Dharmesh Shah, Dr.

+91(120)256-9779

dharmesh.shah@pharmazz.com

CONTACT