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Preoperative Data and the Spinal Spread of Local Anesthetic in Cesarean Section

NCT07197398 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2025-09-29

No results posted yet for this study

Summary

This study is designed to assess possible relation between the anthropometric data of pregnant women at term, as well as their babies, and the maximal level of sensory blockade following spinal anesthesia for cesarean section. The debate regarding this relation is ongoing. Although there is some relevant data in favor of both lack and the presence of significant relation between these variables, it is still not clear whether the same dose of local anesthetic is similarly effective, regardless of parturient's and fetal size.

Conditions

  • Spinal Anesthesia Evaluation
  • Cesarean Delivery

Interventions

OTHER

Spinal block level analysis

Relation of pregnancy - related, maternal and neonatal data to the level of sensory blockade in the whole study group will be assessed. Only cases with 12.5mg of hyperbaric bupivacaine will be included.

OTHER

Data collection

Intervention is to retrieve and analyse anonymous perioperative data. After identification of eligible cases, statistical analysis will be performed

OTHER

Sub-group analysis

Relation of pregnancy - related, maternal and neonatal data to the level of sensory blockade in the sub-groups of different height (\<165cm and \>165cm) will also be performed.

Sponsors & Collaborators

  • Centre of Postgraduate Medical Education

    lead OTHER

Principal Investigators

  • Małgorzata Malec-Milewska, MD, Prof. · Department of Anesthesia and Intensive Care, Orlowski Hospital, Warsaw

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-18
Primary Completion
2025-11-30
Completion
2025-11-30

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07197398 on ClinicalTrials.gov