Comparison of Dural Puncture Epidural Versus Conventional Epidural for Labour Analgesia in Primig… (NCT06766812) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Comparison of Dural Puncture Epidural Versus Conventional Epidural for Labour Analgesia in Primigravida
60 participantsStarted 2025-01-15
Plain-language summary
This study aims to compare the analgesic efficacy and safety of the Dural Puncture Epidural (DPE) technique versus the Conventional Epidural (CE) technique for labor analgesia in primigravida.
Who can participate
Age range
18 Years – 40 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Primigravida women aged 18-40 years.
. Gestational age between 37 and 42 weeks.
. Single pregnancy with vertex presentation.
. Patients in active labor with cervical dilation of less than 5 cm at the time of epidural placement.
. American Society of Anesthesiologist physical status I or II.
. Patients who provide informed consent for participation in the study.
Exclusion criteria
. Patients with contraindications to neuraxial anesthesia (e.g., coagulopathy, infection at the puncture site).
. History of preeclampsia, gestational diabetes, or any other significant medical conditions that could influence labor or anesthesia outcomes.
. Patients with a history of previous uterine surgery, including cesarean section.
. Known fetal anomalies or non- vertex presentations.
. Patients with morbid obesity (BMI \> 40 kg/m²).
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.