Magnesium Sulfate and Postoperative Hypercoagulability in Laparoscopic Gynecological Surgeries
Launched by MARIANNA MAVROMATI · Nov 30, 2024
Trial Information
Current as of July 01, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how magnesium sulfate, a common medication, affects the blood's tendency to clot after laparoscopic gynecological surgeries, which are minimally invasive surgeries performed on women. The goal is to find out if magnesium sulfate can help prevent excessive blood clotting after these surgeries, a condition known as hypercoagulability. The study will involve women aged 18 and older who are classified as ASA I or II, meaning they are generally healthy or have mild health issues. Participants must also be taking preventive blood-thinning medications before and after their surgery.
If you or someone you know is considering participating in this trial, you can expect to be part of a double-blind study, meaning neither you nor the researchers will know who is receiving magnesium sulfate and who is getting a placebo (a non-active substance). The study is currently recruiting participants, and it's important to note that certain health conditions, like severe obesity, pregnancy, or serious medical issues, would exclude someone from participating. This trial aims to improve the safety and care of women undergoing these types of surgeries by understanding how magnesium sulfate may help manage blood clotting.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • ASA I and II patients
- • Laparoscopic gynecological surgeries
- • age \>18 years
- • Patients receiving prophylactic anticoagulant therapy 12 hours before surgery based on the Caprini score
- • Patients receiving prophylactic anticoagulant therapy 12 hours postoperatively based on the Caprini score.
- Exclusion Criteria:
- • ASA ≥ III
- • age \<18 years
- • BMI \>40 kg/m²
- • Pregnancy
- • Known hematologic disorders
- • Liver/kidney/cardiovascular disease
- • Severe anemia (6,5- 7,9 g/dl)
- • Inability or refusal to provide informed consent
About Marianna Mavromati
Marianna Mavromati is a dedicated clinical trial sponsor with a focus on advancing innovative healthcare solutions through rigorous research and development. With a commitment to ethical practices and patient safety, Mavromati oversees a portfolio of clinical trials aimed at evaluating the efficacy and safety of novel therapies. Her extensive expertise in clinical operations and regulatory compliance ensures that each trial adheres to the highest standards, fostering collaboration among interdisciplinary teams to drive scientific discovery and improve patient outcomes. Through her leadership, Marianna Mavromati is dedicated to contributing to the evolving landscape of medical science.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Athens, Attica, Greece
Patients applied
Trial Officials
Kassiani Theodoraki, Professor
Study Chair
Aretaieio University Hospital, National and Kapodistrian University of Athens
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported