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IRCT20180607040003N1 IRCT 2018-09-03 Gonabad University of Medical Sciences Effect of intravenous aminophylline on post- spinal anesthesia headache in women under cesarean section Effect of intravenous aminophylline on post- spinal anesthesia headache in women under cesarean section 2018-04-21 anticipated 70 Complete https://irct.ir/trial/33442 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Randomization description: Available sampling from all women candidates for cesarean section with spinal anesthesia referred to Razi Torbat Heydarieh Hospital and Allameh Bhlol Gonabadi Hospital in Gonabad city, after being eligible for inclusion criteria by random allocation method using blocks Reversal, so that the number 1 as an intervention group (the group receiving aminophylline 3 mg based on the ideal body weight and 500 ml normal saline 0.9% venous) and the number 2 as the control group (receiving group 500 C C is considered to be 0.9% venous saline), and 4-block blocks (eg 2121) in the theme, Blinding description: In this study, the patients in the intervention group, after obtaining informed consent and entering the study, are not aware of which amniotic fluid injectable serum are available. Also, the clinical caregiver of the intervention group is unaware. Only the researcher has prepared the serum and the name of the patient in the intervention group and It will provide control to the clinical care provider for infusion, as well as assessing the outcome of the pain, the clinician will do without the knowledge of the intervention and control group. 1 Headache. Intervention 1: Intervention group: Headache before giving aminophylline in the aminofilin dose group. In this study, 3 cc per kg body weight of the drug are given at the diagnosis of the headache, and after an hour the patient is examined by the doctor and the healing It is recorded. Intervention 2: Control group: For patients in the control group, only 500 cc normal saline 0.9% intravenous infusion is infused over 2 hours. Undecided - It is not yet known if there will be a plan to make this available Justification or reason for indecision in sharing IPD is Do not information
public hoseyn bayeste
Asian Roadside Border
gonabad Iran (Islamic Republic of) 9691793718 +98 51 5222 6013 m.eshaghzadeh93@gmail.com Gonabad University of Medical Sciences scientific hoseyn bayesteh
Asian Roadside Border
gonabad Iran (Islamic Republic of) 9691793718 +98 51 5722 3028 m.eshaghzadeh93@gmail.com Gonabad University of Medical Sciences Iran (Islamic Republic of) Satisfaction to participate in the study Subjected to cesarean section with spinal anesthesia No history of sensitivity to aminophylline or other xanthine derivatives with accurate history from them. Age 45-18 years Lack of history of migraine headaches, coagulation disorders, gestational toxicity, diabetes, seizure, smoking and narcotics, and cardiovascular diseases 18 years 45 years Female Performing a retinal anxiety Unwillingness to cooperate in the study General anesthesia Use of xanthine derivatives during the study G44 Other headache syndromes Treatment - Drugs Treatment - Drugs Intervention group: Headache before giving aminophylline in the aminofilin dose group. In this study, 3 cc per kg body weight of the drug are given at the diagnosis of the headache, and after an hour the patient is examined by the doctor and the healing It is recorded. Control group: For patients in the control group, only 500 cc normal saline 0.9% intravenous infusion is infused over 2 hours. Headache. Timepoint: 24h. Method of measurement: observation. Gonabad University of Medical Sciences Approved 2017-12-17 Gonabad University of Medical Sciences Asian Roadside Border gonabad Razavi Khorasan Iran (Islamic Republic of)