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Clinical Trials in Israel / NCT06235749
Recruiting Not applicable

Administration Of Calcium Gluconate for The Reduction of Blood Loss During Elective Cesarean Delivery

NCT06235749 · tracked via the Priya Life Science Israel tracker
Phase
Not applicable
Started
2023-11-14
Last updated
2026-07-16

Condition(s) studied

Elective Cesarean Delivery

Investigational drug(s) / intervention(s)

Calcium Gluconate 10% →sodium chloride 0.9%

Calcium Gluconate 10%: Administration of Calcium Gluconate 10% IV following umbilical cord clamping

sodium chloride 0.9%: Administration of sodium chloride 0.9% IV following umbilical cord clamping

Study summary

Postpartum hemorrhage (PPH) is the leading cause of death related to pregnancy. PPH can lead to blood transfusion, disseminated intravascular coagulation (DIC), hysterectomy, or death. The prophylactic administration of uterotonic agents as part of an active management of the third stage of labor has been proven to reduce rates of PPH. However, even with these treatments, PPH rate is still relatively high, and puts women at risk of heavy bleeding and death.

Calcium is a key component in the coagulation cascade and known as factor IV. It has a role in platelet activation, and it is an important co-factor for the activation of factors II and There is a concentration-dependent effect of hypocalcemia on in vitro clot strength in patients at risk of bleeding. Calcium gluconate is the calcium salt of gluconic acid, and it has a relatively strong safety profile.

Hypocalcemia is a poor prognostic factor in actively bleeding patients. Calcium has a positive inotropic effect both on skeletal muscle and smooth muscle. The inotropic effect doesn't skip the myometrium, and it is well-established that hypocalcemia can impair myometrial contractility. As so, calcium channel blockers are prescribed as a tocolytic drug and calcium gluconate should be considered as adjuvant therapy for treating PPH duo to atony, in case of prolonged tocolytic or magnesium sulfate use prior to delivery. Studies have already shown an association between low ionized calcium levels and the risk for severe bleeding. In a pilot randomized controlled trial of patients with risk factors for uterine atony, calcium was shown to reduce uterine atony compared to placebo. However, current studies have small sample size and are limited to a high-risk population. There are no recommendations in current guidelines for monitoring calcium levels or prescribing calcium as a prophylactic measure for the third stage of labor, despite atony and coagulopathy being significant causes of PPH.

HYPOTHESIS: Administration of Calcium Gluconate at the third stage of elective Cesarean delivery will decrease the rates of blood loss during and after the surgery by reducing the rates of uterine atony and development of coagulopathy, thus has the potential of reducing the incidence of PPH and its complications without severe side effects.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: \- Elective Cesarean Delivery, at Gestational age of 35 weeks or more. Exclusion Criteria: * Age younger than 18 years old. * Patients treated with calcium channel blockers. * Chronic renal failure and hyperphosphatemia. * Sarcoidosis. * Hypocalcemia (ionized Ca\<1 mmol/L) or hypercalcemia (ionized Ca\> 1.3 mmol/L) before the surgery. * Any QT abnormalities as evident by ECG before Calcium Gluconate administrations or any known conduction abnormality.

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Soroka Medical Center Beersheba Israel Recruiting
Shamir Medical Center Be’er Ya‘aqov Israel Recruiting
Rambam Medical Center Haifa Israel Recruiting
Edith Wolfson Medical Center Holon Israel Recruiting

More Rambam Health Care Campus trials in Israel

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06235749 on ClinicalTrials.gov ↗ ← All trials in Israel