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Tests treatment safety and results for Labor Analgesia
Official title The Effect of Ultrasound Real-time Guidance Technique on the Effectiveness and Safety of Labor Analgesia
ClinicalTrials.gov ID: NCT06300151
What this study is testing
- What it's testing
- Ultrasound real-time guidance technology has great advantages over traditional blind exploration technology in terms of accuracy, success rate, and reduction of puncture damage in intervertebral space positioning through operational visualization, greatly improving the effectiveness and safety of spinal block. At present, Doppler ultrasound is rarely used for spinal block, especially for real-time ultrasound guidance technology, which has not been widely applied in clinical practice due to its high equipment requirements, lack of mature puncture plans, complex operation, and high learning curve.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 20 to 45, women only
You may be able to join if
- American Society of Anesthesiologists (ASA) Class I or II;
- Single healthy pregnancy;
- Head showing first;
- 37 to 41 weeks;
- The labor process is active, and the cervix dilates\<5cm;
You likely can't join if
- Presence of pregnancy diseases, such as pregnancy hypertension, pre eclampsia, pregnancy diabetes;
- Contraindications to intraspinal analgesia: 1) Central nervous system diseases. 2) Infection or septicemia at the puncture site. 3) Coagulation...
- Known cases of fetal malformation or increased risk of cesarean section, such as a history of uterine rupture;
- Persons with a history of mental illness, hysteria, epilepsy, etc. who cannot cooperate.
- Patients with long-term use of opioids, steroids, and chronic pain.
See the full eligibility criteria
- American Society of Anesthesiologists (ASA) Class I or II;
- Single healthy pregnancy;
- Head showing first;
- 37 to 41 weeks;
- The labor process is active, and the cervix dilates\<5cm;
- Require epidural labor analgesia;
- Volunteer to participate in this study and sign an informed consent form.
- Presence of pregnancy diseases, such as pregnancy hypertension, pre eclampsia, pregnancy diabetes;
- Contraindications to intraspinal analgesia: 1) Central nervous system diseases. 2) Infection or septicemia at the puncture site. 3) Coagulation dysfunction;
- Known cases of fetal malformation or increased risk of cesarean section, such as a history of uterine rupture;
- Persons with a history of mental illness, hysteria, epilepsy, etc. who cannot cooperate.
- Patients with long-term use of opioids, steroids, and chronic pain.
The study team makes the final eligibility decision.
Where it's taking place
- Fuzhou, Fujian, China
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 20 years to 45 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Fuzhou, Fujian, China. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.