Comparison of Epidural Labor Analgesia With Dexmedetomidine or Sufentanil

Status Recruiting

Clinical Trial Summary

The participants: 1800 full-term primiparas will be selected with ASA I-Ⅱgrade, 20 to 35 years old and weighing 55 to 90 kg in the investigator's hospital from may 2018 to December 2018. 1200 primiparas were divided into A and B according to the computer randomized numbers, and 600 parturients without labor analgesia in the same period were selected as group C, with 600 patients in each group. All parturients signed the informed consent form and were approved by the hospital ethics Committee.

Clinical Trial Description

1200 primiparas were divided into A and B according to the computer randomized numbers, and 600 parturients without labor analgesia in the same period were selected as group C, with 600 patients in each group. All parturients signed the informed consent form and were approved by the hospital ethics Committee. ;

Study Design

Related Conditions & MeSH terms

Pharmacological Action

Clinical Trial Details

NCT number	NCT03622047
Study type	Interventional
Source	Fudan University
Contact	zeyong yang, MD, PhD
Phone	86-21-64070434
Email	zeyongy2018@aliyun.com
Status	Recruiting
Phase	N/A
Start date	August 15, 2018
Completion date	August 1, 2020

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