Delivery by elective caesarean section. Delivery by elective caesarean section
Conditions
Interventions
Intervention 1: Intrathecal injection of 75mg lidocaine+ 2.5 µg sufentanil in group A(42 patients). Intervention 2: Intrathecal injection of 60mg lidocaine+2.5 µg sufentanil in group B(42 patients). I
Treatment - Drugs
Intrathecal injection of 75mg lidocaine+ 2.5 µg sufentanil in group A(42 patients).
Intrathecal injection of 60mg lidocaine+2.5 µg sufentanil in group B(42 patients).
Intrathecal injection of 50mg lidocaine+2.5µg sufentanil in group C(42 patients).
Sponsors
Vice Chancellor for Research Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: Exclusion criteria: All patients who are not class I and II ASA; Patients not signed the informed consent; Patients with underlying disease; Patients with chronic pain or; Who have used analgesic medications in the past forty eight hours; Patients with abscess or local infection at the injection site; Severe agitation; Cerebral disorder; Severe psychological disorders and addiction;
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of pain. Timepoint: every three minute after procedure. Method of measurement: Visual analogue Scale.;Nausea and Vomiting. Timepoint: Two and twenty four hours postoperative. Method of measurement: have, or not have. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood Pressure. Timepoint: Once before spinal then every three minute after procedure with Datascope, Model: Pse-420. Method of measurement: mm Hg.;Heart Rate. Timepoint: Once before spinal then every three minute after procedure with Datascope model: Pse-420. Method of measurement: Number per minute. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactParisa Golfam
Kermanshah University of Medical Sciences
Outcome results
None listed