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Effect of epidural catheter depth on labor analgesia after dural puncture epidural technique (DPE): a double-blinded, randomized, controlled trial

Phase 1
Conditions
ull-term expectant mother giving birth to a single baby naturally
Registration Number
ChiCTR2400089022
Lead Sponsor
Department of Anesthesiology, The First Affiliated Hospital of Shantou University Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

1:   Full-term women in singleton pregnancy<br>2:   Age 18-40 years<br>3:   ASA grade I-II<br>4:   cervical dilation <5cm<br>5:   subjects normal delivery process<br>6:   The subject had her own condition and voluntarily received epidural labor analgesia.

Exclusion Criteria

1:   History of drug and food allergies<br>2:   Important systemic diseases such as severe respiratory diseases, pregnancy complicated with severe chronic diseases, or heart disease<br>3:   Pregnant women with platelet count below normal, coagulation dysfunction, or undergoing anticoagulant therapy<br>4:   If the basal temperature before delivery analgesia is above 37.5 ? or has been clearly diagnosed as an infected person<br>5:   There are contraindications to epidural anesthesia<br>6:   Morbid obesity or body mass index = 40kg/m2

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Block the highest plane;whether the subject's anesthesia plane can reach T6 plane and the time to reach T6 plane;
Secondary Outcome Measures
NameTimeMethod
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