Premature Labour Clinical Trial
Official title:
Premature Labour Screening by Cervical Ultrasound for Asymptomatic Pregnant Women in the PACA Region. Various Treatment Strategies : 1. Progesterone 200mg (Vaginal Way) 2. Pessary 3. Vaginal Stitching 4. Rest
State of the question and research objective: International trials have shown that
ultrasound measurement of the cervix identifies a population at high risk of preterm
delivery. In case of short neck several types of treatments can be recommended:
progesterone, the establishment of a strapping or pessary. These three treatments reduce the
risk of preterm delivery. There is no French study.
The objective of this study is to reduce prematurity in the PACA region Monaco-Corsica by
introducing a routine ultrasound screening strategy asymptomatic short necks.
Population concerned: All patients with active singleton pregnancy between 16 and 26 SA SA
are eligible to ultrasound of the cervix.
- Primary endpoint: delivery rate before 37 weeks.
- Criteria secondary judgments rate of deliveries before 37 weeks, neonatal mortality
morbidity.
Expected result: a prematurity of 50%
State of the question and research objective: International trials have shown that
ultrasound measurement of the cervix identifies a population at high risk of preterm
delivery. In case of short neck several types of treatments can be recommended:
progesterone, the establishment of a strapping or pessary. These three treatments reduce the
risk of preterm delivery. There is no French study.
The objective of this study is to reduce prematurity in the PACA region Monaco-Corsica by
introducing a routine ultrasound screening strategy asymptomatic short necks.
Expected result: a prematurity of 50%
Population concerned: All patients with active singleton pregnancy between 16 and 26 SA SA
are eligible to ultrasound of the cervix.
Method of observation and deduction investigation: Study before / after comparing two
periods: period A (2013) and Period B (2015).
- Primary endpoint: delivery rate before 37 weeks.
- Criteria secondary judgments rate of deliveries before 37 weeks, neonatal mortality
morbidity.
Data flow mode:
Duration and terms of organization of research: The actual duration of the study
(preparation and implementation, monitoring and inclusions) is set at 36 months. This study
will be conducted in the context of networks. All maternity hospitals belonging to these
networks will be invited to participate. Referents investigating doctors will be appointed.
The attaché of clinical research in collaboration with the Network Coordinator, Michele
Marcot, get back the data for the year 2013 by the transfer records examination, delivery
specifications, reviews of the hospitalization mother and child.
Data collection for 2015 will be based on a collection form that will complement the
investigators involved in the project at the inclusion of the patient.
These sheets will be collected in real time by the RCAF in charge of monitoring the study
will proceed to their seizure.
Positive cases (short necks - less than 25mm) will be offered or not progesterone treatment,
banding or the establishment of a pessary according to the habits of the practitioner and
the service protocol.
If treatment with progesterone is retained, it is Vaginal Progesterone 200mg, natural
micronized progesterone without excipients with known effect in capsule form.
Data Analysis Method: Statistical analysis will be initiated only after verification of the
validity of the database (queries broadcast from clinicians involved in the study,
consistency checks). There is a procedure and data anonymization algorithm giving each
individual a number. A lookup table is available, separate from the operating base. Only the
number will be entered into the computer database. The database will then be frozen. After
the base gel, the consolidated data will be processed by the statistician. Data analysis
will be performed using the SPSS Version 17.0 software for Windows by the statistician of
the Unit for Clinical Research Methodology (Loundou Anderson, head Prof. Pascal Auquier).
Statistical significance tests will be set at 5%. The type of unilateral or bilateral test
will depend on the chosen alternative, especially based on the results already available in
previous studies.
The qualitative variables are expressed in terms of numbers and percentages, and
quantitative variables will be reported using the usual parameters of position (mean,
median) and dispersion (standard deviation, range). The normality of the distributions of
quantitative data will be systematically searched using the Shapiro-Wilks test. If variables
are not normally distributed, conventional processing techniques (logarithmic, ...) will be
implemented.
Initially, a comparability study populations for inclusion will be made on all the variables
collected at that time: socio-demographic and clinical (using Mantel-Haenszel test, the
Chi-2 or accurate Fisher for qualitative variables, and Student's t test or ANOVA for
quantitative variables) to reveal potential confounding factors to consider when analyzing
the criteria of judgment. Comparisons between the study populations will also be conducted
on all the criteria of secondary judgments. Adjustments will be made on the variables
identified as confounding factors by conducting multivariate analysis (analysis of variance,
multivariate logistic regression).
Justification of the number of subjects or power analysis: The prematurity rate was 7.4% in
2013 in France (PACA, Périnat data 2010).
We expect a reduction in this rate of 1.5 points (or 6%) over the period 2015 referring to
the reduction of prematurity obtained by Kiss, et al, 2003.
To achieve this reduction in preterm birth rate, include 3500 patients in each period.
Considering the selection criteria and the active files of the various partners, the
inclusion of patients in the period 3500 2014 is quite achievable.
(44,000 births per year at the network level, among which are ensuring that 10% of them meet
the predefined criteria). Regarding the second period, the reasoning is the same; among the
list of eligible patients, a random draw will be conducted to determine the 3500 patients
representing this period. Thus for 3500 patients included in the period 2014, 10% will have
a short neck or 350 patients who will be offered the Progesterone, a banding or the
establishment of a pessary.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02338830 -
Vaginal Progesterone for Prevention of Preterm Labor in Asymptomatic Twin Pregnancies With Sonographic Short Cervix
|
Phase 4 | |
| Recruiting |
NCT02673359 -
Vaginal Progesterone Versus Cervical Cerclage for Pregnant Women With Short Cervix and History of PTL and/or MTM
|
Phase 4 |