Survey on Pregnant Women's Knowledge of Pain Relief Procedures During Childbirth
Evaluation of Preexisting Information Regarding Neuroaxial Procedures for Labour Analgesia
This study is trying to find out what pregnant women know about pain relief options like epidurals before they talk to an anesthesiologist.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Goethe University Academic / other |
| Locations | 1 site (Frankfurt am Main, Hesse) |
| Trial ID | NCT06201936 on ClinicalTrials.gov |
What this trial studies
This project aims to anonymously survey pregnant patients about their prior knowledge of neuroaxial analgesia procedures, such as epidurals, before they meet with an anesthesiologist. The study will evaluate the sources of information that these patients have encountered regarding potential complications and side effects of these procedures. By conducting an online survey, the research seeks to identify misconceptions and clarify existing contradictory information that may affect informed consent during labor and delivery.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women who are approaching delivery.
Not a fit: Women under 18 years of age will not benefit from this study as they are excluded from participation.
Why it matters
Potential benefit: If successful, this study could enhance patient understanding and informed consent regarding pain relief options during childbirth.
How similar studies have performed: While this approach is observational and focuses on patient knowledge, similar studies have highlighted the importance of informed consent and patient education in medical procedures.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Pregnant women prior to delivery Exclusion Criteria: * Women under 18 years of age
Where this trial is running
Frankfurt am Main, Hesse
- University Hospital Frankfurt — Frankfurt am Main, Hesse, Germany (Recruiting)
Study contacts
- Study coordinator: Armin N Flinspach, MD.
- Email: armin.flinspach@kgu.de
- Phone: 00496963015868
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.