Evaluation of pain in patients after cesarean section with spinal anesthesia by marcaine and dexmedetomidine.
Conditions
Interventions
Intervention 1: Intervention group: Patients undergoing spinal anesthesia with marcaine 5% (10 mg) + dex duodenomidine diluted 0.5 cc (5 micrograms) will be 2.5 cc in total. The needle used is a Quink
Sponsors
Birjand University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Having informed consent to enter the study ASA Class 1 and 2 Term pregnancy Singleton Non-emergency cesarean section
Exclusion criteria
Exclusion criteria: Drug addiction Dissatisfaction with spinal anesthesia Duration of surgery more than 1 hour Pregnancy with ASA 3 and above Patients with head trauma Patients with spinal deformity Inability to position the patient Infection in site of spinal anesthesia Hypersensitivity to local anesthetic drugs High ICP Coagulation disorders and heart valve problems (especially AS)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determine the average pain score. Timepoint: Immediately after regaining consciousness and 1, 2, 3, 4, 8 and 12 hours after surgery. Method of measurement: Using visual-auditory assessment (VAS) criteria by the study leader. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: immediately after recovery and 1, 2, 3, 4, 8 and 12 hours after surgery. Method of measurement: Sphygmomanometer.;Pulse beats. Timepoint: immediately after recovery and 1, 2, 3, 4, 8 and 12 hours after surgery. Method of measurement: Physical examination. patients' pulse is counted in one minute. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBibi fateme Shakhs Imampoor
Birjand University of Medical Sciences
Outcome results
None listed