CClinicalTrials.gg
Status unknownNCT00939744EAU2Updated Mar 4, 2015

Study of the Effect of Eicosanoids on Contractile Activity of Pregnant Human Myometrium in Pathological Situation

An observational study in Obstetric Labor Complications and Prolonged Pregnancy, sponsored by Université de Sherbrooke. Status unknown at 1 site in Canada. Open to female participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2015-03-04.

Sponsored by Université de Sherbrooke · Observational

The sponsor has not verified this record recently (last verified Mar 2015), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
130
Ages
18 Years to 40 Years
Sex
Female
01

Study summary

Recent studies show that EET and 20-HETE have important biological effects, particularly in the vascular system. The investigators studied the effect of eicosanoids on the gravid rat uterus. The results suggest that 20-HETE had an tocolytics effect on gravid uterus. In the previous study, we demonstrated that the enzymes of the pathway of EET were present in human uterine tissues. Moreover, the addition of an inhibitor of degradation of EET had an tocolytic effect on the human myometrium, as the exogenous addition of 8.9, 14,15-EET and 20-HETE.

Objectives:

Primary objective: To compare the balance of different metabolic pathways of arachidonic acid (AA) of the pregnant human myometrium in pathological situations (preterm labor, uterine atony, prolonged pregnancy).

Specific objectives: i) To study the effect of derived from the AA on in vitro contractile activity of normal and pathological uterine tissues, and ii) detect and quantify the different sub-products of metabolism of AA in the uterine tissues (myometrium, fetal membranes and placenta).

The management of uterine contraction is in the heart of modern obstetrics year, yet the progress made in other specialties, based on the study of smooth muscle have not yet been transposed in obstetrics. A better understanding of systems for regulating the contraction is important in terms of 1) new physiological knowledge, but it could also be the source of 2) modification of strategies to take care of premature delivery (new Tocolytic), or 3) improving the efficiency of uterine muscle during delivery or 4) for treatment of patients with prolonged pregnancy.

Read the detailed description

It is a clinical study with a slope fundamental aims to examine the metabolic pathways of AA of human myometrium and their functional roles according to their clinical profile divided into three contractile pathological situations - threat of premature delivery, dynamic dystocia, prolonged pregnancy - and two groups of patients at term: a group before work and group work.

The sampling method. After birth, a biopsy will be perform from the lower segment of the uterus. After caesarean sections of membrane and placenta are collected.

The substances studied during isometric tension tests are part of the three degradation pathways of the AA.

  1. new eicosanoids in cumulative dose (8,9-EET, 11,12-EET, 14,15-EET, 20-HETE), and in combination
  2. enzyme inhibitors of the eicosanoids pathway (AUDA, MS-PPOH, DDMS), and the COX and LOX pathways (indomethacin), alone or in combination.
02

Conditions studied

  • Obstetric Labor Complications
  • Prolonged Pregnancy

Keywords

  • contractile activity
  • eicosanoids
  • pregnant women
  • obstetrics complications
03

In context

Obstetric Labor Complications

89 studies on the registry are indexed under Obstetric Labor Complications; 25 are open to participants now.

This study's planned enrollment of 130 is below the median of 178 across 26 observational studies indexed under Obstetric Labor Complications.

Browse Obstetric Labor Complications studies →

Lead sponsor

Université de Sherbrooke is the lead sponsor of 289 studies on the registry; 68 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

women who will have a c-section at the CHUS

Inclusion criteria

  • all women who will have a c-section

Exclusion criteria

Exclusion Criteria:

  • induction of labor,
  • child with malformation,
  • birth weight less than 2500 grams or greater than 4500g
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
130 participants (estimated)
Biospecimen retention
Samples without dna

Groups and cohorts

  • EAU2

    Women who will have a c-section at the CHUS

06

What researchers measure

Primary outcomes

  1. effect of eicosanoids on contractile activity of myometrium of pregnant women with pathological situations

    Time frame: during c-section

Secondary outcomes

  1. effect of enzymatic inhibitors on contractile activity of myometrium from pregnant women with pathological situations

    Time frame: during c-section

  2. detection of enzymes from the different pathways

    Time frame: after c-section

  3. quantification of eicosanoids in different tissues

    Time frame: after c-section

07

Study locations

1 of 1 sites recruiting
  • Centre hospitalier de l'Université de Sherbrooke
    Sherbrooke, Quebec J1H 5N4, Canada
    Recruiting
08

References and documents

Publications

  • Corriveau S, Pasquier JC, Blouin S, Bellabarba D, Rousseau E. Chronic levothyroxine and acute T3 treatments enhance the amplitude and time course of uterine contractions in human. Am J Physiol Endocrinol Metab. 2013 Mar 1;304(5):E478-85. doi: 10.1152/ajpendo.00346.2012. Epub 2012 Dec 18. PubMed 23249699 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00939744
Lead sponsor
Université de Sherbrooke
Collaborators
Fonds de la Recherche en Santé du Québec
Responsible party
Jean-Charles Pasquier, MD, PhD (Dr, Université de Sherbrooke) — Principal investigator
First posted
Jul 15, 2009
Start date
May 2009
Primary completion
Jul 2015 (estimated)
Completion
Oct 2015 (estimated)
Last update
Mar 4, 2015

Study contacts

Stéphanie Corriveau, BSc
Contact
stephanie.corriveau@usherbrooke.ca
819 346-1110 ext. 13875
Simon Blouin, PhD
Contact
syblouin.chus@ssss.gouv.qc.ca
819 346-1110 ext. 13877
Jean-Charles Pasquier, MD, PhD
principal investigator · Centre hospitalier de l'Université de Sherbrooke
Rousseau Éric, PhD
principal investigator · Université de Sherbrooke

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion