Health Condition 1: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Intervention1: Nil: Nil
Intervention2: Nil: Nil
Sponsors
Christian Medical College
Eligibility
Inclusion criteria
Inclusion criteria: ASA physical status 2 singleton pregnant mothers over 145 cm in height with no comorbidities or well-controlled comorbidities with normal placentation, undergoing elective lower segment caesarean section at full term
Exclusion criteria
Exclusion criteria: Mothers with high-risk pregnancy, multiple pregnancy, or uncontrolled comorbidities. Mothers who undergo lower segment caesarean section under general anesthesia, or those who have failed spinal anesthesia. Mothers who have chronic pain syndrome, allergy to opioids, fetal or placental anomalies. Mothers undergoing preterm or post-term caesarean delivery. Mothers who have postpartum hemorrhage and those who received additives other than morphine 100mcg
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of analgesia post intrathecal Morphine as indicated by duration to first patient requested analgesia is the primary outcome.Timepoint: Duration of analgesia post intrathecal Morphine as indicated by duration to first patient requested analgesia is the primary outcome. | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of respiratory depression defined as respiratory rate less than 10Timepoint: immediate post operative period;Incidence of sedation as described by RASS sedation scaleTimepoint: Immediate post operative period;Incidence of post operative nausea and vomitingTimepoint: 48 hours post operatively;Incidence of post operative pruritusTimepoint: 48 hours after intrathecal morphine administration;Duration to flatusTimepoint: Time from intrathecal morphine administration to passing flatus first | — |
Countries
India
Contacts
Public ContactSamCharles
Christian Medical College, Vellore
Outcome results
None listed