NCT04693572

Brief Summary

The purpose of this study is to examine the anesthetic considerations and outcomes during repeated caesarean section and to compare such considerations in low-order vs high-order repeated caesarean sections.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2021

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 31, 2020

Completed
1 day until next milestone

Study Start

First participant enrolled

January 1, 2021

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 5, 2021

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2021

Completed
Last Updated

January 5, 2021

Status Verified

December 1, 2020

Enrollment Period

11 months

First QC Date

December 31, 2020

Last Update Submit

December 31, 2020

Conditions

AnesthesiaPregnancy, High RiskPregnancy Related

Keywords

Caesarian SectionRepeated Caesarian SectionAnesthesia

Outcome Measures

Primary Outcomes (2)

  • Percentage of sections performed under general anesthesia

    1 day

  • Percentage of in-surgery conversion from regional to general anesthesia

    1 day

Study Arms (1)

Parturients undergoing repeated caesarean sectiona

Eligibility Criteria

Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Parturients undergoing repeated caesarean section.

You may qualify if:

  • Parturients undergoing repeated caesarean section.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Jacob Weinstein, MD

CONTACT

+972544302909jacobweins@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
4 Weeks
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Fellow

Study Record Dates

First Submitted

December 31, 2020

First Posted

January 5, 2021

Study Start

January 1, 2021

Primary Completion

December 1, 2021

Study Completion

December 1, 2021

Last Updated

January 5, 2021

Record last verified: 2020-12