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Respiratory Rate After Cesarean Delivery

NCT04250233 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2023-04-19

No results posted yet for this study

Summary

The study proposal summarizes aspects related to respiratory rate in women who undergo spinal anesthesia for cesarean delivery who receive or do not receive neuraxial opioids

Conditions

  • Cesarean Delivery; Neuraxial Opioids

Interventions

DEVICE

Respiratory Monitor

All women receive a respiratory rate monitor after cesarean delivery. We anticipate that at least 30 women will receive standard dose neuraxial block, and aim to have a cohort of 20-30 women who receive non-standard dose (Group 20 in order to compare respiratory rates.

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-11
Primary Completion
2023-03-26
Completion
2023-03-26

Countries

  • Israel

Study Locations

More Related Trials

Entities

Companies

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 NCT04250233 on ClinicalTrials.gov