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Procedure

Accuro ultrasound for Cesarean Section

N/A
Waitlist Available
Research Sponsored by Brigham and Women's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, average of 3 hours
Awards & highlights

Study Summary

This study is evaluating whether ultrasound imaging can help reduce the number of needle redirections needed to perform spinal anesthesia.

Eligible Conditions
  • Cesarean Section
  • Spinal Anesthesia
  • Lumbar Ultrasound

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, average of 3 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, average of 3 hours for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of Needle Redirections
Secondary outcome measures
Number of Needle Passes
Patient Satisfaction with procedure
Procedural Time

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Accuro ultrasoundExperimental Treatment1 Intervention
Group II: ControlPlacebo Group1 Intervention

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Who is running the clinical trial?

Brigham and Women's HospitalLead Sponsor
1,605 Previous Clinical Trials
11,467,186 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Pre-Insertion Ultrasound for Lateral-Position Spinal in Cesarean Delivery
Naida Margaret Cole 2021. "Pre-Insertion Ultrasound for Lateral-Position Spinal in Cesarean Delivery". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04592926.
~28 spots leftby Apr 2025
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