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Clinical Trials/RBR-8xdc8yz
RBR-8xdc8yz
Not yet recruiting
Phase 2

Randomized clinical trial to evaluate the safety and pharmacodynamics of the PARP inhibitor Olaparib in sepsis - PARP Poly [ADP-ribose] polymerase

Escola Paulista de Medicina, Universidade Federal de São Paulo0 sitesDecember 30, 2022

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Escola Paulista de Medicina, Universidade Federal de São Paulo
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 30, 2022
End Date
December 15, 2024
Last Updated
2 years ago
Study Type
Intervention
Sex
Male

Investigators

Sponsor
Escola Paulista de Medicina, Universidade Federal de São Paulo

Eligibility Criteria

Inclusion Criteria

  • Male patients diagnosed with septic shock for less than 24 hours; signing of free and informed consent form

Exclusion Criteria

  • Female patients (women) because women's hormones can alter the effects of olaparib; patients unable to use medication by mouth or by tube; patients with AIDS; patients using immunosuppressive therapy, that is, which compromises the body's defenses; patients using corticosteroids; patients with cancer or undergoing chemotherapy; chemotherapy performed up to 30 days; patients who had cardiac arrest; patients with recent acute infarction or problems with the coronary artery, the artery that supplies the heart; liver disease, such as liver cirrhosis; very severe patients, with the prospect of death within 24 hours; palliative or end\-of\-life care; patients using treatments that may have their effects altered or alter the effects of olaparib (examples: itraconazole, fluconazole, verapamil, rifampicin, phenytoin, carbamazepine, phenobarbital and modafinil; Saint John's herb)

Outcomes

Primary Outcomes

Not specified

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