Progesterone in the Treatment of Acute Hemorrhagic Stroke

NCT ID: NCT04143880

Last Updated: 2019-11-27

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 184 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-02-01
• Study Completion Date: 2020-12-31

Brief Summary

A large number of preclinical studies have confirmed that progesterone and its metabolites have strong neuroprotective effects. As a neuroprotective agent, progesterone has been effective in several animal models of nerve injury, suggesting that the drug has a wide range of neuroprotective effects. Pharmacodynamic studies have shown that some characteristic mechanisms of the action of the neurosteroid on brain injury and cerebral congestion include: prevention of inflammatory reaction and cell death (by inhibiting the activation of inflammatory cytokines and microglia); control of angiogenic brain edema (by reestablishing blood-brain barrier and regulating aquaporin-4 water transporter) and cytotoxic edema (by regulating Progesterone can also improve the neural dysfunction after cerebral hemorrhage, promote the regeneration and repair of damaged axons (activate PI3K / Akt pathway to inhibit the expression of RhoA), prevent the loss of Ca2 + caused by excitotoxicity and improve the survival rate of neurons. It was found that progesterone injection could reduce brain edema and promote the recovery of nerve function after brain injury.

Detailed Description

The purpose of this clinical trial is to further evaluate the safety and effectiveness of progesterone in the clinical application of major cerebral congestion diseases. The Second Affiliated Hospital of Zhejiang University is the unit in charge of clinical research, and six units participate in the multicenter randomized, double-blind, placebo-controlled clinical trial.

Conditions

Stroke

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

experimental group

Progesterone

Group Type: EXPERIMENTAL

Progesterone

Intervention Type: DRUG

intramuscular injection intranasal administration

control grou

saline

Group Type: PLACEBO_COMPARATOR

saline

Intervention Type: OTHER

intramuscular injection intranasal administration

Interventions

Progesterone

intramuscular injection intranasal administration

Intervention Type: DRUG

saline

intramuscular injection intranasal administration

Intervention Type: OTHER

Other Intervention Names

progesterone injection

Eligibility Criteria

Inclusion Criteria

• Acute hemorrhagic stroke was confirmed by CT or MRI. There should be no obvious sequelae symptoms in the first stroke or previous stroke, Mrs < 2 (slight or no neurological dysfunction).
• Patients aged 40-80 (male, menopausal women);
• Patients with 6-48 hours of onset;
• 3 points ≤ NIHSS score ≤ 15 points for light and medium patients;
• Patients or family members sign informed consent.

Exclusion Criteria

• Cerebral CT has excluded intracranial hemorrhage, and there is no imaging change of early large area cerebral infarction.
• Pregnant or lactating women;
• Previous intracranial hemorrhage, including suspected subarachnoid hemorrhage; large area stroke (> 2 / 3 MCA territory) or head CT showed any degree of midline displacement due to brain edema. Signs of intracranial hemorrhage (ICH, SAH, extradural hemorrhage, acute or chronic SDH) were found on baseline CT or MRI scan.
• Fever, defined as central body temperature > 37.5 ℃;
• Patients with severe heart, liver and kidney dysfunction or severe diabetes;
• Platelet count was less than 100 × 109 / L, blood glucose was less than 27 mmol / L, serum creatinine was more than 2.0 mg / dL or 180 μ mol / L.
• Blood pressure: systolic pressure > 180 mmHg, or diastolic pressure > 100 mmHg;
• Those who have previous allergic history to progesterone and citicoline;
• The anticoagulant has been taken orally, and INR is more than 15; heparin has been taken within 48 hours (APTT is beyond the normal range);
• Participating in clinical trials of any other treatment;
• Patients considered by the researchers not suitable for inclusion.

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Korea University Anam Hospital

OTHER

Sponsor Role: collaborator

Seoul National University Hospital

OTHER

Sponsor Role: collaborator

Lishui Country People's Hospital

OTHER

Sponsor Role: collaborator

Jinhua Central Hospital

OTHER

Sponsor Role: collaborator

Huzhou Central Hospital

OTHER

Sponsor Role: collaborator

The Affiliated Hospital of Hangzhou Normal University

OTHER

Sponsor Role: collaborator

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

YANWQ001

Identifier Type: -

Identifier Source: org_study_id