Clinical Trials Directory

Trials / Completed

CompletedNCT00202722

Remifentanil as Intravenous Patient-controlled Analgesia (IVPCA) During Labour

Remifentanil as Analgesia for Labour Pain

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Sorlandet Hospital HF · Other Government
Sex
Female
Age
Healthy volunteers
Accepted

Summary

Remifentanil is a ultra short-acting synthetic opioid. It is rapidly metabolized by non-specific blood and tissue esterases. We wanted to investigate the efficacy and safety of remifentanil used as analgesia during labour. Intravenous patient controlled analgesia (ivpca) were used to administer remifentanil. Doses used were 0,15-1,05 mikrogr/kg, with a lock-out time of 2 minutes. 41 women were included in the study. Blood-pressure, heartrate, SaO2, respiration rate and sedation were recorded every 15.minute. Fetal heart rate was recorded for the whole periode of treatment (CTG, STAN). Vaginal contraction pain were assessed by the parturients every 15.minute using a Visual Analogue Scale (VAS). Midwives also recorded their impression of the parturients pain. The parturients level of sedation were recorded by anesthesiologist and midwife every 15.minute. Apgar scores were registered at 1, 5 and 10 min after delivery. Umbilical cord blood analysis regarding blood gases and concentration of remifentanil were performed. After delivery, both mother and midwife evaluated efficacy and safety; Global satisfaction score, if the remifentanil doses were sufficient, nausea, vomiting, level of sedation and dizziness.

Detailed description

Primary and secondary outcome measures presented under "results"

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilIntravenous patient controlled analgesia (ivpca) during labour

Timeline

Start date
2004-01-01
Primary completion
2007-07-01
Completion
2007-08-01
First posted
2005-09-20
Last updated
2014-06-23
Results posted
2014-06-23

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT00202722. Inclusion in this directory is not an endorsement.