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Reduction of Spontaneous Prematurity by Antibiotic Treatment (Josamycin) (PREMYC)

Primary Purpose

Prematurity

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Josamycin
Placebo
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prematurity focused on measuring Prematurity, Ureaplasma spp, Mycoplasma Hominis, Amniotic fluid, Josamycine

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient older ≥ 18 years
  • French speaking
  • Women who have an amniocentesis between 15 and 20 weeks of amenorrhoea for an antenatal diagnosis
  • Affiliated to social security or an equivalent system
  • Karyotype analysis and ultrasound morphological normal (apart from minor signs of trisomy 21)
  • Clear amniotic fluid (not contaminated by the mother's blood)
  • Gestational age is between 15 WA(day+0) and 20 WA(day+6)
  • Patient have not allergy to macrolides
  • Do not have cure underway by macrolide
  • Patient followed during her pregnancy in an investigator site
  • Informed consent and signed

Exclusion Criteria:

  • No speaking french
  • Having an allergy to macrolides
  • Having a multiple pregnancy
  • Morphological Anomaly
  • Patient no consented
  • Lactose Intolerance
  • Not agreed to participate

Sites / Locations

  • Groupe Hospitalier Chenevier-Mondor, CHI

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

josamycin

Placebo

Outcomes

Primary Outcome Measures

Premature birth

Secondary Outcome Measures

Antenatal :occurence of a miscarriage late
Antenatal : premature delivery
Antenatal : hospitalisation for risk of premature delivery
antenatal : Number of day of hospitalisation for risk of premature delivery
Antenatal : premature rupture of membranes
Antenatal : occurence of chorioamnionitis defined by 2 of the following criteria :maternal temperature > 38°C, uterine contractions, Fetid leucorrhoeas, foetal tachycardia > 160bpm, C reactive protein >10mg/l
During childbirth : Hyperthermia > 38°C
During childbirth : fetal tachycardia > 160 bpm
Post-partum : Hyperthermia > 38°C for more than 24hours
Post partum :need an antibiotic treatment for more than 48 hours
Neonatal : neonatal mortality late
Neonatal : early neonatal mortality
Neonatal morbidity : immediate neonatal state
Neonatal morbidity : infection
Neonatal morbidity : respiratory disease
Neonatal morbidity : digestive disease

Full Information

First Posted
July 17, 2008
Last Updated
December 27, 2011
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Bayer
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1. Study Identification

Unique Protocol Identification Number
NCT00718705
Brief Title
Reduction of Spontaneous Prematurity by Antibiotic Treatment (Josamycin)
Acronym
PREMYC
Official Title
Reduction of Spontaneous Prematurity: Impact of Antibiotic Treatment (Josamycin) in Case of Positive PCR for Ureaplasma Spp and/or Mycoplasma Hominis in Amniotic Fluid
Study Type
Interventional

2. Study Status

Record Verification Date
May 2011
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Bayer

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test the effectiveness of an antibiotic treatment (Josamycin) in the case of positive PCR for Ureaplasma spp. and/or Mycoplasma hominis in the second quarter on the risk of premature birth.
Detailed Description
Infection would be the cause of 40 % of spontaneous premature deliveries. The physiopathological hypothesis accepted is a premature ascent of present bacteria in the low genital ways towards the decidual, the foetal membranes then the amniotic liquid. These bacteria are responsible for an inflammatory reaction to the interface feto-maternal characterized by the production of proinflammatory cytokines and pro-contractants agents (prostaglandins, oxytocin) by the decidual and the membranes. These mediators cause uterine contractions, a maturation of the uterine collar, a rupture of the membranes then a premature birth. Several recent publications show on the one hand that Mycoplasma hominis and Ureaplasma spp. are the bacteria most frequently found in the amniotic liquid in the second quarter of the pregnancy and that a positive PCR for these bacteria is associated with a premature birth. A probable assumption would be that Mycoplasma hominis or Ureaplasma spp. cause a premature birth by infecting the fetal membranes and the decidual, then activating the immune system and the pro-inflammatory production of cytokines. These bacteria are sensitive to antibiotic treatment. Nevertheless, no randomized controlled trials have been carried out to determine wether an antibiotic treatment would decrease spontaneous prematurity in the case of positive PCR in the amniotic liquid.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prematurity
Keywords
Prematurity, Ureaplasma spp, Mycoplasma Hominis, Amniotic fluid, Josamycine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
3200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
josamycin
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Josamycin
Intervention Description
josamycin with posology of 2 grams per day by oral way during 10 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo with posology of 2 grams per day by oral way during 10 days
Primary Outcome Measure Information:
Title
Premature birth
Time Frame
between 22 and 37 completed weeks of pregnancy.
Secondary Outcome Measure Information:
Title
Antenatal :occurence of a miscarriage late
Time Frame
between 16 and 22 weeks of amenorrhoea
Title
Antenatal : premature delivery
Time Frame
at week of amenorrhea <= 34, 32, 28
Title
Antenatal : hospitalisation for risk of premature delivery
Time Frame
antenatal period
Title
antenatal : Number of day of hospitalisation for risk of premature delivery
Time Frame
antenatal period
Title
Antenatal : premature rupture of membranes
Time Frame
before 37 week of amenorrhea
Title
Antenatal : occurence of chorioamnionitis defined by 2 of the following criteria :maternal temperature > 38°C, uterine contractions, Fetid leucorrhoeas, foetal tachycardia > 160bpm, C reactive protein >10mg/l
Time Frame
antenatal period
Title
During childbirth : Hyperthermia > 38°C
Time Frame
Childbirth period
Title
During childbirth : fetal tachycardia > 160 bpm
Time Frame
childbirth period
Title
Post-partum : Hyperthermia > 38°C for more than 24hours
Time Frame
post partum period
Title
Post partum :need an antibiotic treatment for more than 48 hours
Time Frame
post partum period
Title
Neonatal : neonatal mortality late
Time Frame
from day 7 to day 28
Title
Neonatal : early neonatal mortality
Time Frame
from day 0 to day 6
Title
Neonatal morbidity : immediate neonatal state
Time Frame
neonatal period
Title
Neonatal morbidity : infection
Time Frame
neonatal period
Title
Neonatal morbidity : respiratory disease
Time Frame
neonatal period
Title
Neonatal morbidity : digestive disease
Time Frame
neonatal period

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient older ≥ 18 years French speaking Women who have an amniocentesis between 15 and 20 weeks of amenorrhoea for an antenatal diagnosis Affiliated to social security or an equivalent system Karyotype analysis and ultrasound morphological normal (apart from minor signs of trisomy 21) Clear amniotic fluid (not contaminated by the mother's blood) Gestational age is between 15 WA(day+0) and 20 WA(day+6) Patient have not allergy to macrolides Do not have cure underway by macrolide Patient followed during her pregnancy in an investigator site Informed consent and signed Exclusion Criteria: No speaking french Having an allergy to macrolides Having a multiple pregnancy Morphological Anomaly Patient no consented Lactose Intolerance Not agreed to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gilles KAYEM
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Groupe Hospitalier Chenevier-Mondor, CHI
City
Creteil
ZIP/Postal Code
94
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
30403730
Citation
Kayem G, Doloy A, Schmitz T, Chitrit Y, Bouhanna P, Carbonne B, Jouannic JM, Mandelbrot L, Benachi A, Azria E, Maillard F, Fenollar F, Poyart C, Bebear C, Goffinet F. Antibiotics for amniotic-fluid colonization by Ureaplasma and/or Mycoplasma spp. to prevent preterm birth: A randomized trial. PLoS One. 2018 Nov 7;13(11):e0206290. doi: 10.1371/journal.pone.0206290. eCollection 2018.
Results Reference
derived

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Reduction of Spontaneous Prematurity by Antibiotic Treatment (Josamycin)

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