Clin2
NCT06235749Possibly a fitRecruiting

Calcium gluconate to reduce bleeding during planned C-section

Elective Cesarean Delivery

Part of Women’s health & pregnancy clinical trials.

This study tests whether giving calcium gluconate during a planned cesarean can reduce blood loss. It may be an option for women who are at least 35 weeks pregnant and have no conditions that affect calcium or heart rhythm.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,180 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are scheduled for a planned (elective) cesarean delivery.
  • Your pregnancy is at least 35 weeks (35 weeks or more).
  • You are 18 years old or older.
  • You are not taking a calcium channel blocker (like nifedipine, verapamil, or diltiazem).
  • You do not have chronic kidney failure, high phosphate levels, or sarcoidosis.
  • Your calcium levels are normal before surgery, and you have no known heart rhythm problems.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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