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Recruiting NCT07500519

NCT07500519 Preoperative Shock Indexes and Post-Spinal Hypotension in Cesarean Surgery

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Clinical Trial Summary
NCT ID NCT07500519
Status Recruiting
Phase
Sponsor Marmara University
Condition Spinal Anesthesia
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2025-10-15
Primary Completion 2026-08-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 300 participants in total. It began in 2025-10-15 with a primary completion date of 2026-08-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This prospective observational study aims to evaluate the predictive performance of preoperative Shock Index (SI) and Modified Shock Index (MSI) for hypotension following spinal anesthesia in elective cesarean surgery. Post-spinal hypotension is a common complication that can affect maternal and fetal outcomes, and early identification of at-risk patients is essential for effective perioperative management.

Eligibility Criteria

Inclusion Criteria: * Patients over 18 years old * ASA II-III patients undergoing elective cesarean section Exclusion Criteria: * ASA IV patients * Patients with known neurologic or psychiatric disorders * Patients with clinically significant cardiovascular, respiratory, hepatic, renal or metabolic disease * Patients with alcohol or drug addiction * Mentally disabled patients * Patients with BMI\>30 * Patients who develop massive bleeding or coagulopathy

Contact & Investigator

Central Contact

Beliz Bilgili

✉ belizbilgili@gmail.com

📞 +905362187927

Frequently Asked Questions

Who can join the NCT07500519 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Spinal Anesthesia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07500519 currently recruiting?

Yes, NCT07500519 is actively recruiting participants. Contact the research team at belizbilgili@gmail.com for enrollment information.

Where is the NCT07500519 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07500519 clinical trial?

NCT07500519 is sponsored by Marmara University. The trial plans to enroll 300 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology