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The Effect of Ultrasound Real-time Guidance Technique on the Effectiveness and Safety of Labor Analgesia

The Effect of Ultrasound Real-time Guidance Technique on the Effectiveness and Safety of Labor Analgesia - Ultrasound Real-time Guidance Technique

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082498
Enrollment
Unknown
Registered
2024-03-29
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor analgesia

Interventions

Ultrasound Real-time Guidance combined with Dural Puncture Epidural Group:Ultrasound Real-time Guidance combined with Dural Puncture Epidural labor analgesia

Sponsors

fujian provincial hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion 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.

Exclusion criteria

Exclusion criteria: ?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 vaginal delivery or uterine rupture after cesarean section; ?Persons with a history of mental illness, hysteria, epilepsy, etc. who cannot cooperate. ?Patients with long-term use of opioids, steroids, and chronic pain.

Design outcomes

Primary

MeasureTime frame
Analgesic effect(onset time);Analgesic effect(block level);Analgesic effect(Visual Analogue Scale);Analgesic effect(Patient controlled analgesia);Uterine contraction indicators(Frequency);Uterine contraction indicators(duration);Fetal heart indicators(Fetal heart rate);Apgar score;Fetal heart indicators(NICHD classification);Analgesic effect(block effect);Uterine contraction indicators(Tachysystole);Uterine contraction indicators(hypertonus);Fetal heart indicators(Fetal Heart Rate decelerations);Fetal heart indicators(Fetal Heart Rate Variability);Sacral sensory block;modified bromage score;

Secondary

MeasureTime frame
Operation evaluation(time);Operation evaluation(number of times);Operation evaluation(side effects and Complications);Delivery mode;Laboratory indicators(Interleukin 6);Laboratory indicators(hypersensitive C-reactive protein);Laboratory indicators(cortisol);Maternal rehabilitation indicators(Postpartum hospital stay);Maternal rehabilitation indicators(Edinburgh Postnatal Depression Scale);Maternal rehabilitation indicators(Postoperative Recovery Quality Scale);Adjust the treatment plan;Drug consumption;Effect of stages of labor(time);body temperature changes;Infection during labor;Side effects and complications of labor analgesia;The reasons and number of pregnant women with conversion of natural labor to Caesarean section;Self-Rating Anxiety Scale;Delivery fear score(numerical rating scale);Delivery satisfaction survey;

Countries

China

Contacts

Public ContactZongxun Lin

fujian provincial hospital

13763820916@189.cn+86 137 6382 0916

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026