Clinical Trials Directory

Trials / Completed

CompletedNCT00710086

Intravenous Remifentanil for Labor Analgesia

Remifentanil Intravenous Patient-controlled Labor Analgesia for Nulliparous Women

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
1,000 (actual)
Sponsor
Nanjing Medical University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Labor analgesia is an essential health caring procedure for women. However, epidural analgesia cannot be performed on all subjects for different contraindications, such as lower platelet counter, back infection at the puncture site, and fear of epidural injection etc. Therefore, intravenous analgesia is an alternative for such conditions. Given the influence of intravenous administration of drugs on fetus, the drug selection is very important. Remifentanil, a super-short efficacious opioid, can last for 3-4 minutes after injection, which is similar in both maternal and fetal environment. Thus the fetus-associated side effects would be less than other drugs. The investigators hypothesized that remifentanil would be a superior intravenous drug used with patient-controlled technique for labor analgesia.

Conditions

Interventions

TypeNameDescription
DRUGHydromorphoneIntravenous administration of hydromorphone 1mg at the patient's request if they felt uterine contraction pain
DRUGRemifentanilRemifentanil intravenous PCA: 0.2μg/kg, lockout time interval 2 minutes, continuous infusion rate 0.2-0.8μg/kg/min.

Timeline

Start date
2008-07-01
Primary completion
2009-09-01
Completion
2009-09-01
First posted
2008-07-04
Last updated
2009-09-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00710086. Inclusion in this directory is not an endorsement.