ClinicalTrials.Veeva

Menu

LXRs, Cholesterol Metabolism and Uterine Dystocia

C

Centre Hospitalier Universitaire de Nīmes

Status

Terminated

Conditions

Uterine Inertia
Dystocia

Treatments

Biological: Whole blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT01107158
2009-A00968-49 (Other Identifier)
AOI/2009/KM-01

Details and patient eligibility

About

Despite the fact that a link between cholesterol and the myometrium has been clearly established, no study investigating aspects of cholesterol metabolism and uterine dystocia currently exists. This study is a pilot study whose aim is to test the hypothesis that an association between uterine dystocia and single-nucleotide polymorphisms (SNPs) in the genes coding for the LXRs.

Enrollment

58 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing C-section for a dystocia: 2 to 3 hours of stagnation in labor progress are observed (ie no increasing dilation, and uterine contractions less that 3-5 per 10 minutes) in spite of measures taken to overcome dystocia (oxytocin injection and artificial breaking of waters)
  • the child is alive
  • the child does not have apriori known malformations that could interfere with a vaginal birth
  • foetus in cephalic position
  • full term pregnancy (>= 37 weeks of amenorrhea)
  • single birth
  • patient has signed consent
  • patient is affiliated with a social security system

Exclusion criteria

  • vaginal birth
  • programmed C-section
  • C-section is chosen because the fetus has a cardia rhythm problem, and there is no stagnation in the labor process
  • multiple pregnancy
  • the child is in a breech position
  • premature birth (<37 weeks amenorrhea)
  • in utero fetal death
  • fetal malformation known before birth that could interfere with a vaginal birth
  • non french-speaking patient (impossible to correctly inform the patient)
  • patient under guardianship

Trial design

58 participants in 2 patient groups

Group 1
Description:
Control group: these patients have mechanical dystocia; cholesterol metabolism factors are a priori not involved.
Treatment:
Biological: Whole blood sampling
Group 2
Description:
These patients have uterine dystocia
Treatment:
Biological: Whole blood sampling

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems