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Clinical Trials/CTRI/2023/07/055182
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

Sponsor
AIIMS New Delhi

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