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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04544488
Other study ID # ACCOUPIV
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 28, 2021
Est. completion date October 1, 2022

Study information

Verified date January 2022
Source Poitiers University Hospital
Contact Bertrand GACHON, MD; PhD Student
Phone + 33 5 49 44 39 45
Email bertrand.gachon@chu-poitiers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Severe complications of childbirth are common. Many factors have been studied to assess their imputability in the occurrence of perineal tears. While women subjectively have different push profiles in terms of intensity, frequency and duration of each push effort, no study has evaluated this variability in a relevant, simple and reproducible way. Through this work, it is expected to establish a qualitative evaluation of the expulsive efforts during childbirth in term nulliparous women by measuring the intra bladder pressure which testifies of the pressure exerted on the perineal tissues due to maternal pushing efforts


Description:

Scientific context: It is clearly observed in clinical practice that there seems to be significant variability in the characteristics of the expulsive phase from one woman to another without this being clearly described to date. During the same expulsive phase, the number, intensity and duration of each push can be very different from one woman to another. Considering that during expulsive efforts, the fetal head exerts pressure on the perineal tissues , the repetition of these compressions, moreover if they are prolonged or brought closer together could generate muscular lesions by hyper extension of the fibers, by microtrauma or by tissue hypoxia. These variations in the characteristics of expulsive efforts could thus modify the perineal risk for women. More than the expulsive efforts evaluated by the recording of intra uterine pressures which has already been described, it is the evaluation of the mechanical stresses transmitted to the perineum secondary to the pushing efforts that we would like to record by the installation of a sensor pressure connected to the woman's bladder catheter. Investigations During the second phase of labor, at 8 cm dilation, after information and obtaining free and informed consent, women will be included by one of the MD investigators. 3 visits are planned in the protocol: The first visit will be at childbirth Evaluation of the mechanical stresses transmitted to the perineum secondary to the pushing efforts by the installation of a sensor pressure connected to the woman's bladder catheter Follow up A prospective study including nulliparous term pregnant women with 2 other visits planned at 3 months (12 to 16 weeks) and 6 months (26 to 30 weeks) after delivery, to assess secondary perineal complications


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date October 1, 2022
Est. primary completion date October 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility - Inclusion criteria : - Pregnant women aged of 18 years or more - 37 weeks or more of pregnancy - Without any previous delivery (vaginal or cesarean delivery) - With a cephalic presentation fetus - With epidural analgesia at 8 cm cervical dilatation (inclusion) - - Exclusion criteria: - Pathological pregnancy (intrauterine growth restriction, pre-eclampsia etc.) - Untreated psychiatric disorders - Women under judicial protection - Women without health insurance

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Recording of expulsive efforts by connection of a pressure sensor to the women's bladder probe
Using a pressure probe connected to a Foley Catheter, intra bladder pressure wille be registered during the whole duration of expulsive phase. The device will be inserted into women's bladder using usual guidelines for insertion of Foley catheter

Locations

Country Name City State
France CHU Poitiers Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary characteristics of the pushing efforts assessed by measuring intra bladder pressur At inclusion it will be collect the characteristics of the pushing efforts: the intensity, the duration (total and of each effort) and the frequency of the expulsive efforts, which will be described in terms of mean and standard deviation. Day of inclusion
Secondary Perineal tear According the RCOG Classification Day of inclusion, immediately after delivery
Secondary Clinical pelvic organ mobility POP-Q clinical examination 12 to 16 weeks after inclusion then 26 to 30 weeks after inclusion
Secondary Ultrasound pelvic organ mobility Transperineal pelvic floor ultrasound 12 to 16 weeks after inclusion then 26 to 30 weeks after inclusion
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