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Investigating the effect of ketamine in pain control after cesarean sectio

Phase 2
Not yet recruiting
Conditions
Post-surgery pain.
Other complications of anaesthesia during labour and delivery
O74.8
Registration Number
IRCT20230417057937N1
Lead Sponsor
Shahre-kord University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
120
Inclusion Criteria

Having a term pregnancy and ASA(American Society of Anesthesiologists) class I, II
Participants in the study should refer electively for caesarean section
Consent to participate in the study
Absence of any underlying diseases
Absence of any mental illnesses or mental disorders

Exclusion Criteria

The presence of one of the diseases associated with pregnancy, such as gestational blood pressure or gestational diabetes and fetal problems.
Allergy to ketamine or similar drugs
BMI above 30

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of postoperative pain scores in patients receiving intravenous ketamine and the group receiving normal saline. Timepoint: 0, 30, 60, 90, 120 minutes and 4, 6, 12, 24 hours after cesarean ???????. Method of measurement: Analogue Scale Visual.
Secondary Outcome Measures
NameTimeMethod
Determining the relative frequency of hallucinations in the group receiving intravenous ketamine. Timepoint: 20 minutes after receiving the first dose of medicine. Method of measurement: Based on questions from the patient.;The time required for pain medication after the completion of spinal anesthesia. Timepoint: The first 24 hours after cesarean section. Method of measurement: Time of drug administration.;Apgar score of the newborn. Timepoint: The first and fifth minutes after birth. Method of measurement: It includes 5 components: heart rate, respiratory effort, muscle tone, reflex excitability, color.
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