Clinical trial

Pharmacokinetic Equivalence of Calcium Gluconate and Calcium Chloride in Parturients

Name
70603
Description
Calcium is a life saving medicine in the care of parturients. It has many important uses including treatment of hypocalcemia, treatment of magnesium toxicity, prevention of hypocalcemia during blood transfusion (of citrate containing blood products), treatment of hyperkalemia, and others. Recent clinical trials also suggest that calcium given after cord clamping may decrease blood loss in patients undergoing cesarean delivery. 2 FDA approved forms of calcium can be given intravenously: calcium chloride and calcium gluconate. Over the last decade there have been times with drug shortages of either calcium chloride or calcium gluconate. So there have been and likely will continue to be times when one formulation or the other may not be adequately available. Despite the importance of calcium and the frequency in which it is used in parturients, there are no published studies in parturients to determine dose equivalence between calcium gluconate and calcium chloride. In this study the investigators will determine the population pharmacokinetics of calcium gluconate and calcium chloride in parturients and calculate the dose equivalent ratio the two drugs. This will help clinicians select appropriate doses of calcium and provide resilience to the drug supply chain in our era of frequent drug shortages.
Trial arms
Trial start
2023-08-19
Estimated PCD
2023-12-15
Trial end
2023-12-15
Status
Completed
Phase
Early phase I
Treatment
Calcium Gluconate
Infused intravenously over 10 minutes upon umbilical cord clamping. First 10 assigned patients received 2 grams per protocol. Subsequent 13 patients received 1.5 grams, dose recalibrated per protocol.
Arms:
Calcium Gluconate
Calcium chloride
0.5 grams of calcium chloride, infused intravenously over 10 minutes upon umbilical cord clamping
Arms:
Calcium Chloride
Size
34
Primary endpoint
Bioequivalent ratio of calcium gluconate (g) to calcium chloride (g)
Using data gathered from serial lab draws at 5 minutes, 10 minutes, 15 minutes, 30 minutes, 60 minutes after initiation of infusion
Clearance from first to second compartment (L/min)
Using data gathered from serial lab draws at 5 minutes, 10 minutes, 15 minutes, 30 minutes, 60 minutes after initiation of infusion
Volume of distribution of first compartment of pharmacokinetic model (L)
Using data gathered from serial lab draws at 5 minutes, 10 minutes, 15 minutes, 30 minutes, 60 minutes after initiation of infusion
Clearance from second compartment (L/min)
Using data gathered from serial lab draws at 5 minutes, 10 minutes, 15 minutes, 30 minutes, 60 minutes after initiation of infusion
Volume of distribution of second compartment of pharmacokinetic model (L)
Using data gathered from serial lab draws at 5 minutes, 10 minutes, 15 minutes, 30 minutes, 60 minutes after initiation of infusion
Eligibility criteria
Inclusion Criteria: Pregnant female subjects delivering at the study institution via scheduled cesarean delivery at term (\>=37 weeks gestation) Exclusion Criteria: 1. severe range blood pressure (BP \>160/\>110) within the 48 hours prior to delivery 2. patient age \<18 years or \>45 years 3. renal dysfunction with serum Cr \> 1.0 mg/dL 4. known history of congenital or acquired cardiac disease or history of arrhythmia 5. patient taking digoxin 6. patient currently taking a calcium channel blocker 7. Weight \<55kg or \>100kg, or 8. receiving magnesium infusion within 24 hours prior to or during cesarean delivery 9. administration of intraoperative doses of calcium by the anesthesiology team for clinical indications
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['EARLY_PHASE1'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 34, 'type': 'ACTUAL'}}
Updated at
2024-04-11

1 organization

2 products

4 indications

Indication
Hypocalcemia