CTRI/2023/07/055182Not yet recruitingPhase 1
Efficacy of calcium gluconate in prevention of uterine atony during lower segmental cesarean section delivery: A randomized controlled trial
AIIMS New Delhi0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1)Pregnant female patients (18 to 45 years of age)
- •2)ASA physical class II or III
- •3)Emergency or elective LSCS with risk factors of PPH
- •4)Patients who have atleast two of the following established risk factors for uterine atony: intrapartum Cesarean delivery, failed operative vaginal delivery with forceps or vacuum, magnesium infusion, Chorioamnionitis, multiple gestation, Polyhydramnios, preterm delivery <37 weeks, prior history of postpartum hemorrhage, labor induction or augmentation with oxytocin, advanced maternal age, obesity with body mass index >40.
Exclusion Criteria
- •1)Patient refusal to participate in the study
- •2)Maternal history of cardiac disease, arrhythmias, CAD
- •3)History of renal dysfunction with serum creatinine >1.0 mg/dL
- •4)Patients with placenta accreta
- •5)Treatment with digoxin within the last 2 weeks for a maternal or fetal indication
- •6)Treatment with a calcium channel blocker within 24 hours
- •7)General anaesthesia
Investigators
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