Investigating the effect of dexmedetomidine in TAP block to reduce pain after caesarean section. Pain, unspecified
Conditions
Interventions
Intervention 1: Control group: One group of people (group R) is injected with 20 cc of 0.2% vacaine. Intervention 2: Control group: The other group (RD group) was injected with 20 cc of 0.2% vacaine a
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 38 Years
Inclusion criteria
Inclusion criteria: Pregnant women aged 18-38 are candidates for elective caesarean section and have undergone spinal anesthesia for the operation.
Exclusion criteria
Exclusion criteria: Absence or withdrawal of consent, coagulation disorders, abuse of narcotics and sedatives, history of allergy and drug reaction to the studied drugs, severe mental disorders, conversion of spinal anesthesia to general anesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale (VAS). Timepoint: It will be done 1 hour later, 6, 12 and 24 hours later. Method of measurement: (0 = no pain and 10 = worst imaginable pain) is measured. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean arterial blood pressure (MAP). Timepoint: It will be done at time zero, 1 hour later, 6, 12 and 24 hours later. Method of measurement: Reading from the monitoring device.;Heart beat. Timepoint: It will be done at time zero, 1 hour later, 6, 12 and 24 hours later. Method of measurement: Reading from the monitoring device.;Arterial blood oxygen. Timepoint: It will be done at time zero, 1 hour later, 6, 12 and 24 hours later. Method of measurement: Reading from the monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Moftakhar
Ahvaz University of Medical Sciences
Outcome results
None listed