Labor analgesia. Newborn (suspected to be) affected by maternal anesthesia and analgesia in pregnancy, labor and delivery
Conditions
Interventions
Intervention 1: Control group: In this group, patients undergo a single spinal anesthesia with an intrathecal injection of 10 micrograms of the opioid sufentanil from Abu Raihan Company. The needle us
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Maternal request for labor analgesia Being multiparous (second to fifth labor) Being Term Cervical dilation is equal to 4 cm Normal coagulation state Physical status classification 1 & 2 Availability of normal Non- Stress Test (NST) of fetus
Exclusion criteria
Exclusion criteria: Allergy to dexamethasone Allergy to opioids Pregnant women who are addicted to opioids or illegal drugs Pregnant women with psychiatric diseases Pregnancy with history of diabetes or/and hypertension diseases Pregnant women who are contraindicated for spinal techniques due to Multiple Sclerosis (MS) or other neurological diseases Refuse of pregnant women for doing spinal technique
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of analgesia. Timepoint: Determining the patient's pain score using a visual analog scale (VAS) before the start of the intervention, at 1 and 5 minutes after the intervention, and at 2, 3, and 4 hours after the intervention. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNiloofar Khosravi
Iran University of Medical Sciences
Outcome results
None listed