Neuroaxial Analgesia ProceduresEPIDURALNCT06201936
EPIDURAL- Evaluation of Preexisting Information Regarding Neuroaxial Procedures for Labour Analgesia
An observational study of Neuroaxial Analgesia Procedures, run by Goethe University at 1 site in Germany.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 65 years, women only
- Conditions the study is for
- Neuroaxial Analgesia Procedures
- What is being tested?
- Preliminary information on neuroaxial procedures
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 1,346 participants
- Where
- 1 siteGermany
- Study dates
- 1 Mar 2025to 1 Aug 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- Women only
- Adult, Older adult
Study population: Pregnant women before delivery for whom a neuroaxiual procedure for pain reduction during childbirth would theoretically be eligible.
Who may be able to join
- Pregnant women prior to delivery
Who cannot join
- Women under 18 years of age
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Evaluation of Preexisting Information Regarding Neuroaxial Procedures for Labour Analgesia
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.
Read the detailed description
Within labour and delivery, neuroaxial anaesthesia (peridural or spinal anaesthesia) is commonly used in accordance with clinical practice guidelines. However, from a professional perspective, there are still questionable and incorrect statements about possible complications and side effects that cannot be justified medically. In an increasingly technological and networked society, the dissemination of medical information via various sources of information poses a potentially serious problem in terms of disinformation, and the correct classification of information is becoming more and more difficult.
Anaesthesiologists are increasingly confronted with consultations in which, in addition to the actual informed consent for the intervention, extensive clarification of existing contradictory information is required.
The aim of this research project is to survey pregnant patients prior to receiving an anaesthesiological consultation about their previous knowledge of the intended procedure by conducting an anonymous online survey.
- Conditions
- Neuroaxial Analgesia Procedures
- Being tested
- Preliminary information on neuroaxial procedures
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Preliminary information on neuroaxial proceduresBehavioural
Pre-existing information of pregnant women on neuroaxial pain-relieving procedures for childbirth and their informative sources
What is being measured
The primary outcome is the main question the study is designed to answer.
Preliminary information on neuroaxial analgesic procedures for childbirth
Is prior information available.[yes/no]
Measured: 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]
Measured: Between the 25+0 week of pregnancy and delivery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jan 2024
- Study start1 Mar 2025
- Primary completion1 Aug 2026
- Study completion1 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Neuroaxial Analgesia ProceduresStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 1,346 participants (actual)
Sponsor and investigators
- Lead sponsor
- Goethe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Armin N. Flinspach, Goethe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06201936
- Sponsor's protocol ID
- 2023-1XXX
- Acronym
- EPIDURAL
- Status last verified
- Aug 2026
- First submitted
- 2 Jan 2024
- Last updated
- 6 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: This is not possible without major restrictions due to state, national and european data protection legislation.
Study at a glance
From the registry record, last updated by the sponsor on 6 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Preexisting Information Regarding Neuroaxial Procedures for Labour Analgesia
- ClinicalTrials.gov ID
- NCT06201936
- Acronym / sponsor ID
- EPIDURAL / 2023-1XXX
- Conditions
- Neuroaxial Analgesia Procedures
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,346 participants (actual)
- Lead sponsor
- Goethe UniversityUniversity, hospital or other
- Study start
- 1 Mar 2025 (actual)
- Primary completion
- 1 Aug 2026 (actual)
- Study completion
- 1 Aug 2026 (actual)
- First posted
- 11 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Within labour and delivery, neuroaxial anaesthesia (peridural or spinal anaesthesia) is commonly used in accordance with clinical practice guidelines. However, from a professional perspective, there are still questionable and incorrect statements about possible complications and side effects that cannot be justified medically. In an increasingly technological and networked society, the dissemination of medical information via various sources of information poses a potentially serious problem in terms of disinformation, and the correct classification of information is becoming more and more difficult.
Anaesthesiologists are increasingly confronted with consultations in which, in addition to the actual informed consent for the intervention, extensive clarification of existing contradictory information is required.
The aim of this research project is to survey pregnant patients prior to receiving an anaesthesiological consultation about their previous knowledge of the intended procedure by conducting an anonymous online survey.
Study design
- Observational model
- Other
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 65 years
- Sex
- Female only
- Age groups
- Adult, Older adult
- Study population
- Pregnant women before delivery for whom a neuroaxiual procedure for pain reduction during childbirth would theoretically be eligible.
Key inclusion criteria (1 listed)
- Pregnant women prior to delivery
Key exclusion criteria (1 listed)
- Women under 18 years of age
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Preliminary information on neuroaxial proceduresPre-existing information of pregnant women on neuroaxial pain-relieving procedures for childbirth and their informative sources | Behavioural | – |
Primary outcome
Preliminary information on neuroaxial analgesic procedures for childbirth
Time frame: Between the 25+0 week of pregnancy and delivery
Is prior information available.[yes/no]
Is the prior information based on internet sources?
Time frame: Between the 25+0 week of pregnancy and delivery
Is prior information available based on a internet sources.[yes/no]
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Aug 2026.
- Individual participant dataSharing planned: No. This is not possible without major restrictions due to state, national and european data protection legislation.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Neuroaxial Analgesia Procedures, run by Goethe University at 1 site in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Preliminary information on neuroaxial analgesic procedures for childbirth (time frame: Between the 25+0 week of pregnancy and delivery). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Aug 2026.