Abstract
Originalsprog | Engelsk |
---|---|
Tidsskrift | American Journal of Obstetrics and Gynecology |
Vol/bind | 200 |
Udgave nummer | 6 |
Sider (fra-til) | 627.e1-10 |
ISSN | 0002-9378 |
DOI | |
Status | Udgivet - 2009 |
Bibliografisk note
Keywords: Adult; Double-Blind Method; Female; Gestational Age; Humans; Obstetric Labor, Premature; Oligopeptides; Pregnancy; Receptors, OxytocinAdgang til dokumentet
Citationsformater
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS
I: American Journal of Obstetrics and Gynecology, Bind 200, Nr. 6, 2009, s. 627.e1-10.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
}
TY - JOUR
T1 - The effect of barusiban, a selective oxytocin antagonist, in threatened preterm labor at late gestational age: a randomized, double-blind, placebo-controlled trial
AU - Thornton, Steven
AU - Goodwin, Thomas M
AU - Greisen, Gorm
AU - Hedegaard, Morten
AU - Arce, Joan-Carles
N1 - Keywords: Adult; Double-Blind Method; Female; Gestational Age; Humans; Obstetric Labor, Premature; Oligopeptides; Pregnancy; Receptors, Oxytocin
PY - 2009
Y1 - 2009
N2 - OBJECTIVE: The objective of the study was to compare barusiban with placebo in threatened preterm labor. STUDY DESIGN: This was a randomized, double-blind, placebo-controlled, multicenter study. One hundred sixty-three women at 34-35 weeks plus 6 days, and with 6 or more contractions of 30 seconds duration during 30 minutes, cervical length 15 mm or less, and cervical dilatation > 1 and < 4 cm were randomized to a single intravenous bolus of barusiban (0.3, 1, 3, or 10 mg) or placebo. The primary endpoint was percentage of women who did not deliver within 48 hours. RESULTS: None of the barusiban doses reduced the number of uterine contractions compared with placebo. There was no significant difference in the percentage of women who did not deliver within 48 hours (72% placebo and 65-88% barusiban groups; P = .21-.84). Barusiban was not associated with an adverse safety profile in the woman, fetus, neonate, or infant. CONCLUSION: An intravenous bolus of barusiban was no more effective than placebo in stopping preterm labor in pregnant women at late gestational age.
AB - OBJECTIVE: The objective of the study was to compare barusiban with placebo in threatened preterm labor. STUDY DESIGN: This was a randomized, double-blind, placebo-controlled, multicenter study. One hundred sixty-three women at 34-35 weeks plus 6 days, and with 6 or more contractions of 30 seconds duration during 30 minutes, cervical length 15 mm or less, and cervical dilatation > 1 and < 4 cm were randomized to a single intravenous bolus of barusiban (0.3, 1, 3, or 10 mg) or placebo. The primary endpoint was percentage of women who did not deliver within 48 hours. RESULTS: None of the barusiban doses reduced the number of uterine contractions compared with placebo. There was no significant difference in the percentage of women who did not deliver within 48 hours (72% placebo and 65-88% barusiban groups; P = .21-.84). Barusiban was not associated with an adverse safety profile in the woman, fetus, neonate, or infant. CONCLUSION: An intravenous bolus of barusiban was no more effective than placebo in stopping preterm labor in pregnant women at late gestational age.
U2 - 10.1016/j.ajog.2009.01.015
DO - 10.1016/j.ajog.2009.01.015
M3 - Journal article
C2 - 19306963
SN - 0002-9378
VL - 200
SP - 627.e1-10
JO - American Journal of Obstetrics and Gynecology
JF - American Journal of Obstetrics and Gynecology
IS - 6
ER -