NCT06201936

Brief Summary

The aim of this research project is to anonymously survey pregnant patients before the anaesthesiological consultation about their prior knowledge of planned neuroaxial procedures in the context of childbirth by conducting an online survey and to evaluate the sources of that information.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
6mo left

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress71%
Mar 2025Nov 2026

First Submitted

Initial submission to the registry

January 2, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 11, 2024

Completed
1.1 years until next milestone

Study Start

First participant enrolled

March 1, 2025

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Last Updated

May 7, 2025

Status Verified

April 1, 2025

Enrollment Period

1.4 years

First QC Date

January 2, 2024

Last Update Submit

May 5, 2025

Conditions

Neuroaxial Analgesia Procedures

Outcome Measures

Primary Outcomes (2)

  • Preliminary information on neuroaxial analgesic procedures for childbirth

    Is prior information available.\[yes/no\]

    Between the 25+0 week of pregnancy and delivery

  • Is the prior information based on internet sources?

    Is prior information available based on a internet sources.\[yes/no\]

    Between the 25+0 week of pregnancy and delivery

Interventions

Preliminary information on neuroaxial proceduresBEHAVIORAL

Pre-existing information of pregnant women on neuroaxial pain-relieving procedures for childbirth and their informative sources

Eligibility Criteria

Age18 Years - 65 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnant women prior to delivery
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Pregnant women before delivery for whom a neuroaxiual procedure for pain reduction during childbirth would theoretically be eligible.

You may qualify if:

  • Pregnant women prior to delivery

You may not qualify if:

  • Women under 18 years of age

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Frankfurt

Frankfurt am Main, Hesse, 60590, Germany

RECRUITING

Central Study Contacts

Armin N Flinspach, MD.

CONTACT

00496963015868armin.flinspach@kgu.de

Florian J Raimann, MD.

CONTACT

00496963015868florian.raimann@kgu.de

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Consultant

Study Record Dates

First Submitted

January 2, 2024

First Posted

January 11, 2024

Study Start

March 1, 2025

Primary Completion (Estimated)

August 1, 2026

Study Completion (Estimated)

November 1, 2026

Last Updated

May 7, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

This is not possible without major restrictions due to state, national and european data protection legislation.

Locations

DE(1)