Clinical Trials Directory

Trials / Unknown

UnknownNCT03622047

Comparison of Epidural Labor Analgesia With Dexmedetomidine or Sufentanil

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
1,800 (estimated)
Sponsor
Fudan University · Academic / Other
Sex
Female
Age
22 Years – 42 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidine ropivacaineObserving the effect of 0.5 μ g / ml sufentanil+ 0.1 % ropivacaine with 2 hours after fetal delivery, and the patients leave the delivery room without abnormality.
DRUGNo analgesia laborNo analgesia labor control group

Timeline

Start date
2018-08-15
Primary completion
2020-08-01
Completion
2020-08-01
First posted
2018-08-09
Last updated
2020-02-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03622047. Inclusion in this directory is not an endorsement.