cesarean. Encounter for cesarean delivery without indication
Conditions
Interventions
Intervention 1: Intervention group: Patients in both case and control group will receive 10 mg of 0.5 % bupivacaine plus 100 µg of morphine and 20 ng naloxone of Tolid daru companies intrathecaly. Int
Sponsors
Sari University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: patents admit in Emam hospital For cesarian ASA classification 1or 2 60 -80 Kg weight first or second pregnancy
Exclusion criteria
Exclusion criteria: Patients who used opiate drugs before cesarean section consumption of any medicine to reduce itching unsuccessful spinal anesthesia prolong surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: The pain level will be evaluated at 2, 4, 6 and after 24 hours after surgery. Method of measurement: Visual Analogue Scale(VAS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausia. Timepoint: it will be evaluated at 2, 4, 6 and 24 hours after surgery. Method of measurement: asking the patient.;Itching. Timepoint: will be evaluated at 2, 4, 6 hours after surgery. Method of measurement: asking the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Reza Habibi
Sari University of Medical Sciences
Outcome results
None listed