Application of Electronic Endoscope in Fetal Distress
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: endoscope application.
- Who it may be relevant to
- Registry conditions: Fetal Distress, Fetal Hypoxia. Basic parameters: 20 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The New Application of Electronic Endoscope in the Visual Diagnosis and Treatment of Intrauterine Fetal Distress During Labor
Overview
Fetal distress is a common emergency in obstetrics, which refers to the combined symptoms of fetal health and life in utero due to acute or chronic hypoxia, with an incidence of 2.7% to 38.5%. Fetal distress is mainly related to abnormal amniotic fluid, umbilical cord entanglement and compression, which is an important reason for the increase of cesarean section rate during delivery. At present, the diagnosis of fetal distress mainly relies on electronic monitoring of fetal heart, and the false positive rate is high. Intrauterine pressure catheter has not been widely used because of the little effect of intrauterine treatment and the increase of infection. Endoscopy has been widely used in the diagnosis and treatment of various specialties at present, but the diagnosis and treatment during childbirth are still in a blind area. The characteristics of endoscopic visualization provide a new idea for the diagnosis and treatment of fetal distress during delivery, especially for the etiological diagnosis and treatment of umbilical cord factors. The use of intraauterine endoscope during delivery can make up for the defects of intrauterine pressure catheter, realize the visual diagnosis of the causes of fetal distress such as oligoamniotic fluid, meconium contamination of amniotic fluid, umbilical cord compression caused by entangling and true junction, etc. At the same time, it can also improve the intrauterine environment by perfusion of saline for the causes of fetal embarrassment, correct fetal distress, and extend the observation time during labor. It is beneficial to reduce caesarean section during labor.
Interventions
- Device endoscope application
Intrauterine bronchoscopy application for fetal distress during labor
Primary outcome measures
- fetal distress rate [Time frame: through study completion, an average of 1 year]
Secondary outcome measures (4)
- vaginal delivery rate [Time frame: through study completion, an average of 1 year]
- Incidence of maternal infection [Time frame: through study completion, an average of 1 year]
- Neonatal asphyxia rate [Time frame: through study completion, an average of 1 year]
- neonatal NICU admission rate [Time frame: through study completion, an average of 1 year]
Eligibility criteria
Inclusion criteria
- Subjects aged 20-45 years with single pregnancy;
- Intrauterine fetal distress occurs during labor (during the first stage of labor), and the fetal membrane was already broken;
- Fetal heart monitoring category II, after stopping oxytocin, oxygen inhalation, change of position, intravenous fluid and other measures can not improve;
- Understand the research procedures, be able to follow the procedures of the research protocol, and voluntarily sign a written consent.
Exclusion criteria
- Type III fetal heart monitoring for pregnant women who require emergency c-section
- Pregnant women with GBS positive
- Pregnant women suspected of chorioamniotic infection
- Pregnant women have signs of reproductive system infection (vaginal inflammation, cervicitis, uterine infection)
- Pregnant women suspected of uterine rupture
- Pregnant women with abnormal contractions: excessive strong contractions
- Check the fetus for serious deformities during pregnancy
- Check pregnant women with serious abnormal functions of cardiovascular system, urinary system, digestive system, reproductive system and other organs
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Diagnostic
Study locations
China · 1 center
- First Affiliated Hospital of Nanjing Medical University — Nanjing
Identifiers
NCT: NCT06608654 · EEFD-01