post cesarean complications. Delivery by caesarean section, unspecified
Conditions
Interventions
Intervention 1: Intervention group : In propofol group 0.25 mg/kg will be injected interavenos after clamping of umbilical cord and fetus expulsion. Intervention 2: Intervention group: In ketamin gr
Treatment - Drugs
Intervention group : In propofol group 0.25 mg/kg will be injected interavenos after clamping of umbilical cord and fetus expulsion
Intervention group: In ketamin group 0.25 mg/kg will be injected interavenos after clamping of umbilical cord and fetus expulsion.
Intervention group: In ketofol group 25 mg propofol pulse 25 mg ketamin will be injected interavenos after clamping of umbilical cord and fetus expulsion.
Control group: In placebo group normal saline will be injected interavenos after clamping of umbilical cord and fetus expulsion
Sponsors
Vice Chancellor for research of Ilam University of Medical Science
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: inclusion criteria : age 18-35; term pregnancy; same surgeon and anesthesia; same dose of spinal anesthesia drug. exclusion criteria : administration of general anesthesia drug; systemic disease
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 1,4,8,12 and 24 hrs after surgery. Method of measurement: Visual Analogue Scale (VAS) and checklist.;Shivering. Timepoint: During recovery. Method of measurement: checklist and VAS.;Nausea & Vomiting. Timepoint: During recovery. Method of measurement: checklist and VAS. | — |
Secondary
| Measure | Time frame |
|---|---|
| Brest feeding time. Timepoint: after surgery. Method of measurement: hrs. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMolouk Jaafarpour
Ilam University of Medical Science
Outcome results
None listed