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Table 1 Study schedule of fluoxetine for motor recovery after acute intracerebral hemorrhage (FMRICH) clinical trial

From: Fluoxetine for motor recovery after acute intracerebral hemorrhage (FMRICH): study protocol for a randomized, double-blind, placebo-controlled, multicenter trial

  Screening Visit 1 Visit 2 Visit 3
Informed consent    
Inclusion criteria    
Inclusion/exclusion criteria check    
Vital signsb  
Medical/drug use historyc    
Smoking/drinking status    
Laboratory testsd    
Lipid teste    
Coagulation testsf   
Date of bleeding    
Condition associated with bleedingg    
Date of BCT    
Volume of the hemorrhageh    
Localization of the hemorrhage    
Concomitant medication
Adverse event   
Depression Scale  
Fugl-Meyer Motor Scale  
Patient’s rehabilitation log   
Barthel Index  
Modified Rankin Scale  
Pill count   
  1. aAge, gender, educational level, marital status, occupational status, date of birth, contact address and telephone number. bBlood pressure (mmHg), pulse (beats/minute) and body temperature (°C). cDiabetes Mellitus, hypertension, dyslipidemia. dHemoglobin, hematocrit, red blood cell count, white blood cell count, platelet count, blood urea, nitrogen/creatinine ratio, fasting plasma glucose. eTotal cholesterol (mg/dl), high-density lipoprotein cholesterol (mg/dl), low-density lipoprotein cholesterol (mg/dl), very low-density lipoprotein cholesterol (mg/dl), triglyceride (mg/dl). fInternational Normalized Ratio, prothrombin time, activated partial thromboplastic time. gTrauma, Drugs, bleeding disorder, exercise. hABC/2 method. BCT, Brain Computed Tomography; NIHSS, National Institutes of Health Stroke Scale.