Condition 1: Labor pain. Condition 2: delivery. Single spontaneous delivery Multiple delivery
Conditions
Interventions
Intervention 1: Patients of group one (group receiving continued infusion, 30 patients) will receive the blobs dose of solution that contain bupivacaine 0.125 plus fentanil 3µg/ml (total volume of 1
Treatment - Drugs
Patients of group one (group receiving continued infusion, 30 patients) will receive the blobs dose of solution that contain bupivacaine 0.125 plus fentanil 3µg/ml (total volume of 10 ml) through ca
Patients of group two (30 patients)will receive the blobs dose of 10 ml from solution that contain bupivacaine 125 mg (26 ml bupivacaeine 0.5% and 100 µg fentanyl in 100 ml normal saline through cat
Sponsors
Vice chancellor for reaserch, Tabriz University of Medical Scienses
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: Parturients with 18-40 years of old; parturients with ASA Class I or II; consenting to be including to the study; women with active labor and vertex presentation Exclusion criteria: Parturients with ASA Class III or higher; cardiovascular diseases; respiratory diseases; contraindication for epidural ; presentation other than vertex; patients with chronic pain and use of analgesics; diabetics
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: every 30 minutes from drug adminstration until delivery. Method of measurement: visual analog scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Motor block. Timepoint: every 30 minute from drug adminstration to delivery. Method of measurement: Modified Bromage scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSousan Rasouli
Reaserch center, Tabriz University of Medical Scienses
Outcome results
None listed