A comparison of pethidine/meperidine intramusculary and remifentanil patient-controlled analgesia during labor in Westfriesgasthuis

A comparison of pethidine/meperidine intramusculary and remifentanil patient-controlled analgesia during labor in Westfriesgasthuis - PCA remifentanil during labor

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON30677

Enrollment

274

Registered

2007-10-05

Start date

2007-11-12

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

contraction-pain pain during labour

Interventions

Group A: painrelief with Remifentanil i.v. using PCA Group B: painrelief with Pethidine i.m. (= standard treatment)

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Pregnant and ASA1, women in labor in Westfries gasthuis, planned vaginal delivery, informed consent parturient, a term pregnancy (37+0 till 42+0 weeks), unborn lies in head-down-position, the unborn has no congenital abnormalities

Exclusion criteria

Exclusion criteria: Pregnant woman requesting epidural analgesia or undergoing epidural analgesia, pregnancy is not a term (<37+0 or >42+0 weeks), kwown allergie for remifentanil, paturient who feels she does not have right amount of time to consider enrolling in this study, other fetal positions than head down, fetal congenital abnormalities

Design outcomes

Primary

Measure	Time frame
Patient satisfaction	—

Secondary

Measure	Time frame
Safety for mother and child including: maternal saturation, respiratory rate and bloodpressure, neonatal Apgar scores and saturation. Painrelief, measured by maternal VAS-scores.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)