None listed
Conditions
Interventions
Intervention 1: Intervention group (Epidural analgesia group): The neuroaxial block is performed with epidural needle number 18 G . First, for the test dose: 3 ml of lidocaine 1.5%, 50 µg of fentanyl
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Ability to have a normal vaginal delivery Existence of labor pain and the delivery is in the active phase. Pregnant mother wants to reduce labor pain itself. Consent of the patient and her husbend.
Exclusion criteria
Exclusion criteria: Missing consent of pregnant woman or spouse. Inability of the pregnant to remain motionless while doing work(e.g. Parkinson disease). Coagulation disorder Increased intracranial pressure (SOL). Local infections at the puncture site History of sensitivity to analgesics and other medication used in this investigation Acute lesions of the CNS Hemodynamic Disorders (e.g. hypotension or Hypovolemia). Cardiovascular Diseases that reduce the cardiac output Embryonic distress. GA 40
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fetal heart rate. Timepoint: 5 min before performing the analgesia and then 5, 10, 20,40, 60 min after and then every 30 min until the exit of the fetus. Method of measurement: With the use of the fetal monitor.;Fetal motion. Timepoint: 5 min before performing the analgesia and then 5, 10, 20,40, 60 min after and then every 30 min until the exit of the fetus. Method of measurement: With the use of the fetal monitor.;Apgar scor. Timepoint: After the delivery at the minute 1 and 5. Method of measurement: calculating. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNabiha aldarir
Tabriz University of Medical Sciences
Outcome results
None listed