Calcium Carbonate to Augment Labor Contractions
Weill Medical College of Cornell University · NCT06580782
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 4
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- November 18, 2024
- Record last updated
- October 23, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The investigators think that calcium carbonate can act as an assistive medication to improve contractions during labor.
Being studied: Calcium Carbonate 500 MG; Standard Dose Synthetic Pitocin
Conditions: Labor Dystocia; Labor Induction; Labor Augmentation
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 18 years or older
- Nulliparas (no prior pregnancy lasting 20 weeks or greater of gestation)
- Gestational age above 36 weeks, at enrollment
- Present for induction or augmentation of labor inclusive of medical indication, elective induction at greater than 39 weeks' gestation, trial of labor after cesarean
- Singleton gestation (a multiple gestation reduced to a singleton, either spontaneously or therapeutically, before 14 0/7 weeks of gestation is acceptable)
- Ability to give informed consent
- Planned to undergo initiation of oxytocin infusion by their maternity care provider
Exclusion Criteria
- Unable to understand or read English
- Presence of tachysystole (defined as more than 5 contractions in 10 minutes averaged over 30 minutes), recurrent variable or late fetal decelerations, and bradycardia in the prior 30 minutes before enrollment
- Non-vertex presenting fetus at enrollment
- Planned for cesarean delivery or contraindication to labor by institutional policy (e.g., placenta previa, vasa previa, active genital herpes infection, previous transmural myomectomy)
- Multi-fetal gestation (twins, triplets, and higher order multiples)
- Known contraindication to taking calcium carbonate including renal calculus, high urine calcium levels, elevated serum calcium, low serum phosphate, achlorhydria, or suspected digoxin toxicity.
- Deliveries with fetal chronic and/or pregnancy-related conditions, IUFD (Intra Uterine Fetal Death) or premature \< 36 weeks of gestation.
- Major fetal anomaly suspected prenatally (defined as a fetal anomaly with anticipated neonatal intensive care unit admission)
- Suspected alloimmunization (given the increased likelihood for anticipated neonatal intensive care unit admission)
- Known severe fetal growth restriction (estimated fetal weight \<3rd percentile) or abnormal umbilical artery Doppler studies (given the increased likelihood for anticipated neonatal intensive care unit admission)
- Participation in another interventional study that influences management of labor and delivery or perinatal morbidity or mortality
- Known allergic reactions to synthetic oxytocin intravenous solution or to Calcium Carbonate
- Significantly impaired consciousness or executive function (e.g., intubated or sedated)
- Patients treated with calcium channel blockers such as nifedipine or magnesium.
- Chronic renal failure and hyperphosphatemia.
- Inability to tolerate oral intake (i.e., nausea/vomiting)
Recruiting US locations
Weill Cornell Medicine
New York, NY 10065
Site contact: Ester Sanchez, BSN · 212-746-2106 · ess4006@med.cornell.edu
Study contacts (from the official record)
- Ester Sanchez, BSN · 212-746-2106 · ess4006@med.cornell.edu
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