Clinical Trials Directory

Trials / Completed

CompletedNCT01157325

Cesarean Rate in Parturients Without Neuraxial Analgesia

Comparison of the Cesarean Rate Between Parturients Who Received Neuraxial Analgesia and Those Who Did Not

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
500 (actual)
Sponsor
Nanjing Medical University · Academic / Other
Sex
Female
Age
19 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Currently, it is certain that neuraxial analgesia in early stage of labor and delivery dose not increase the risk of Cesarean section. However, given ethical reasons, whether such a medical procedure could increase the Cesarean rate compared with those who did not received neuraxial analgesia or not is yet to be known. It is difficult to perform such a study in occidental countries because they have a higher rate of labor analgesia. On the contrary, the rate of labor analgesia in China is up to date only 1%, so it can be done easily. The investigators hypothesized that no neuraxial analgesia itself were a risk factor to Cesarean section. Therefore, the investigators design this study to compared the effect of neuraxial analgesia on the rate of Cesarean delivery with those who did not received neuraxial analgesia.

Conditions

Interventions

TypeNameDescription
PROCEDURENeuraxial analgesiaNeuraxial analgesia will be given at any time if the parturient requested analgesia
PROCEDURENon-neuraxial analgesiaNo neuraxial analgesia will be given to those who will not want to an analgesia

Timeline

Start date
2010-07-01
Primary completion
2011-07-01
Completion
2011-07-01
First posted
2010-07-07
Last updated
2011-07-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01157325. Inclusion in this directory is not an endorsement.