Safe Delivery Using a New Device Namely a Belt on the Belly of Pregnant Woman (SDB)

This study has been completed.
Sponsor:
Collaborator:
University of Florence
Information provided by (Responsible Party):
Erich Cosmi MD, PhD, University of Padua
ClinicalTrials.gov Identifier:
NCT01566331
First received: March 19, 2012
Last updated: March 26, 2012
Last verified: March 2012
  Purpose

Safety of natural, vaginal labor for parturient, fetus and newborn is one of most important goal among obstetricians, midwifes, scientific society all over the world. Maternal and newborn clinical problems and complications following vaginal delivery cause a big amount of medico-legal problems and high costs in the sanitary field.

Among the maneuvers that are used in the second stage of labor, uterine fundal pressure is one of the most controversial and often diffuse in all over the world, generally not documented, or under reported in medical records . Many Authors affirms that a different new way to push could be of help. This maneuver was introduced by Kristeller, that in 1867 minutely described a procedure to shorten, through the application of a pressure on the uterine fundus whose intensity was quantified by a dynamometer and the duration measured in seconds, the length of the second phase of the labor. Although uterine fundal pressure maneuver was described by Kristeller as the placement of two hands on the uterine fundus and the consequential application of longitudinal steady pressure at a 30- to 45-degree angle directed toward the pelvis, with the avoidance of direct pressure toward the maternal spine, there is no clear definition of the maneuver and no indication for its use has been formally described to date. Situations in which fundal pressure may be used include non-reassuring fetal heart rate tracings with a need to expedite delivery, assistance with vacuum or outlet forceps delivery in the case of maternal exhaustion, stabilization of the fetal head for artificial rupture of membranes to prevent cord prolapse, or for easier application of a fetal scalp electrode. However, its use continues to be one of the most controversial maneuvers in obstetrics case, due to the maternal and fetal adverse effects attributed to the use of fundal pressure. Manual fundal pressure cannot be measured: that is the reason why could be very dangerous for parturient and/or fetus. This reason together with a "non standardize" manual pushing cause the absence of documentation of the benefits of its use. Indeed, is demonstrated an increased incidence of third- and fourth-degree lacerations (4), hypotension, abdominal bruising, respiratory distress, uterine rupture, fractured ribs and ruptured liver have been reported in the mother, whilst fetal injuries comprise brachial plexus damage, humerous and clavicular fracture, thoracic spinal cord injuries. Moreover, since uterine fundal pressure causes alteration in fetal cerebral blood flow it has been associated also to cerebral palsy and asphyxia complications, as well as to increase of intra-cranial pressure leading to non-reassuring fetal heart rate pattern, umbilical cord compression, hypoxemia, and sub-galeal hemorrhage. Moreover, by forcing a fetal head through the pelvis that would not have passed in the normal process of labor, uterine fundal pressure may also cause shoulder dystocia mainly when that procedure is associated with vacuum and forceps extraction.

The aim of this study was therefore to assess whether the use of the Baby-guardTM system, through its ergonomic, three chamber, inflatable abdominal belt, engineered after studies of biomechanics and biophysics, that follows obstetric semiotics, that applies fundal pressure during the second stage of labor in the direction of the pelvic outlet, may be of maternal and fetus aid for a safe natural childbirth for their better outcomes.


Condition Intervention Phase
Safe Delivery
Device: Baby-guardTM
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Investigator)
Primary Purpose: Supportive Care
Official Title: Safe Natural Delivery by Using a New Inflatable Ergonomic Three Chambers Belt

Further study details as provided by University of Padua:

Primary Outcome Measures:
  • Composite maternal and fetal outcome in pregnant women delivering with Baby Guard Belt device [ Time Frame: 15 days after delivery ] [ Designated as safety issue: Yes ]
    Maternal reduction of pain, reduction of perineal laceration and fetal morbidity and mortality.


Secondary Outcome Measures:
  • Maternal morbidity [ Time Frame: 15 days ] [ Designated as safety issue: Yes ]
    Perineal and cervical lacerations incidence, ; psychological and physical maternal fatigue, maternal request of cesarean section during labor,

  • reduction of second stage of labor and delivery and cesarean section rate [ Time Frame: 15 days ] [ Designated as safety issue: Yes ]
    reduction of second stage of labor and cesarean section rate.


Enrollment: 80
Study Start Date: January 2011
Study Completion Date: March 2011
Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Baby-guardTM
Baby-guardTM system, through its ergonomic, three chamber, inflatable abdominal belt, engineered after studies of biomechanics and biophysics, that follows obstetric semiotics, that applies fundal pressure during the second stage of labor in the direction of the pelvic outlet, may be of maternal and fetus aid for a safe natural childbirth for their better outcomes
Device: Baby-guardTM
Baby-guardTM system, through its ergonomic, three chamber, inflatable abdominal belt, engineered after studies of biomechanics and biophysics, that follows obstetric semiotics, that applies fundal pressure during the second stage of labor in the direction of the pelvic outlet, may be of maternal and fetus aid for a safe natural childbirth for their better outcomes
Other Name: Safety baby guard
No Intervention: no intervention
natural delivery

  Hide Detailed Description

Detailed Description:

A randomized, single blind, controlled, prospective study was performed. Subjects were nulliparous women who delivered at a community setting hospital (U.O.C. Obstetrics and Gynecology, "San Giuseppe" Hospital, Empoli, Italy) between January 24, 2011 and March 24, 2011. Vaginal deliveries were eligible. Patients were therefore divided into two groups by randomly numbered envelopes upon full dilatation of the cervix, and allocated to the following two groups:

  1. The Study Group (n=40 patients) in whom the inflatable belt was applied with the correct pressures (ranging from 80 to 150 mm/Hg, see below the description of the protocol)during Labor and Delivery
  2. The Control Group (n=40 women), in whom the belt was inflated with minimal pressures (from 10 to 20 mm/Hg) During Labor and Delivery To test whether differences between experimental groups are statistically significant, the sample-size should be calculated "a priori". To do this, a primary end-point has been identified: incidence of perineal-cervical lacerations. The sample-size (n > 62 subjects for two groups) will be obtained using STATA program by a two-tailed test [alpha level of 0.05 and 90% of statistical power (1-Beta)], to detect statistically significant reduction from 50% to 10% or less with respect the primary end-point. Therefore a randomized sample size of 40 pregnant women per group was chosen to allow for possible refusals or withdrawals.

Data collected from delivery records, retrospectively obtained and reviewed, will include: patient's age, race, parity, patient's body mass index (BMI, kg/m2) at the time of delivery, and body weight change during pregnancy (defined as the difference between maternal pre-pregnant body weight and body weight at delivery), as part of the ante-partum information. For the intra-partum information, gestational age at delivery, duration of second phase of labor, use of intravenous oxytocin, episiotomy, cervical laceration (as requiring surgical repair for hemostasis), severe perineal lacerations (defined as third- or fourth- laceration, while mild perineal laceration was defend as first- or second- perineal laceration), vacuum extraction, forceps delivery, use of uterine fundal pressure maneuver were abstracted. All The study Group will followed up for 15 days after delivery Fetal weight was estimated by the combination of biparietal diameter, abdominal circumference and femur length. The mean percent difference between the predicted and actual weight was 9.6% corresponding to a mean overestimation of 294 g or underestimation of 314 g. These values are consistent with most reports in the literature.

The study will be performed according to the guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH); the declaration of Helsinki regarding the Standard operating procedures for clinical investigators (GCP); the General requirements for Clinical investigation of medical devices for human subjects. Finally, the local ethical committee approved the study protocol, and all patients received detailed information about the study and the procedure, to which they gave their written consent.

The inflatable belt (Baby-guardTM ) and study protocol The Baby-guardTM (CABEL s.a.s. Costruzioni Elettroniche, Pistoia, Italy) consists of a disposable, ergonomic, three chambers, inflatable belt, and a detector of electro-physiological signals from maternal abdomen (i.e. fetal heart and maternal heart signals - Figure 1). myographic uterine activity). Three chambers that can be separately swollen one from the other in order to repositioning fetal body compose the inflatable belt. The three belt chambers are filled according to the pressures set by the operator (midwife/MD) and allow to gently positioning of the fetus in the wright position towards the pelvis. Once the correct fetal position has been obtained, all three chambers are inflated in synchronously with uterine contraction. The maternal and fetal monitoring unit is composed by a touch-screen computer, that records electro-physiological signals collected by a signal amplifier deriving from the mother (uterine contractions and the maternal heart rate) and the fetus (fetal heart rate and the possibility of Doppler parameters of fetal heart). All parameters and signals detected by the Baby-guardTM system are storable on the touch-screen computer hard disk, as per request of the European Community rules on safety (UNI EN60601)].

This study reports only the part regarding results and outcomes of parturient and neonates.

At the beginning of the uterine contraction, as referred by the patients and revealed by the electro-physiological signals recorded, the midwife/MD, if necessary, inflated 30-50 mmHg of air pressure into the lateral chambers of the inflatable belt to correctly align the fetus avoiding his malpositioning with respect to the pelvis. After monitoring the duration of spontaneous uterine contractions, the midwife/MD therefore inflated from 80 to 150 mm/Hg (for the Study Group) or from 10 to 20 mm/Hg (for the Control Group) of air into the ergonomic belt for 30 sec. Fundal pressure was applied at a 30-40° angle to the spine in the direction of the pelvic outlet through the inflatable belt, standardizing the force and surface area of application (980 cm2). The frequency of inflation was limited to fewer than 6 times per 20 min. followed by a pause of 10 min. All the women, whether randomized to the Study or the Control group, received standard management of the second stage of labor, which includes one-to-one support, fetal heart rate monitoring, and care from midwife. Operative deliveries were performed if clinically indicated. As a uterine contraction started, the inflatable obstetric belt was inflated synchronously and maintained at the pressure above indicated for 30 sec. by the midwife/MD. The Baby-guardTM was not used for more than 2 hours till delivery. The obstetrician, the midwife and the patients were blind to whether the belt was inflated with sufficient pressure (from 80 to 150 mm/Hg for the Study Group) or not (from 10 to 20 mm/Hg for the Control Group).

Outcomes of the study Outcome measures in this study were the perineal and cervical lacerations incidence, the use of uterine fundal pressure maneuver (Kristeller manouvre), the incidence of vacuum extractions, cesarean section incidence during labor, second stage of labor duration; maternal psychological and physical fatigue, maternal request of cesarean section during labor, and absence of neonatal intensive care unit admissions.

At the time of discharge to home, patients' satisfaction with the inflatable belt was evaluated asking them to score about the degree of psychological and physical fatigue with the Baby-guardTM by marking a 10-cm visual analogue scale (VAS) from 0 (minimal) to 10 (optimal). Patients were also asked about the usefulness of the inflatable belt assistance to delivery. The number of cesarean section requests during the second phase of labor was also evaluated.

Statistical analysis All data were analyzed with the STATA software (StataCorp LP, College Station, Texas, USA), and were expressed as mean ± SD (range) or as number (%) of cases. Comparisons of proportions and means between groups (study vs control) were done using the χ2 test (or Fisher exact test, if suitable) and, independent t-test, respectively.

  Eligibility

Ages Eligible for Study:   23 Years to 42 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • women in active labor at term in primipara with maternal age ranging from 23 to 42 years, with a singleton fetus in vertex presentation.
  • the onset of second stage was defined as full dilatation of the cervix identified by digital examination

Exclusion Criteria:

  • preterm labor (gestational age below 37 weeks)
  • breech or transverse presentation
  • suspected fetal macrosomia
  • gestational diabetes
  • pregnancy-induced hypertension
  • abnormalities of placentation (low lying placenta, abruptio placenta)
  • uterine structural abnormalities
  • history of previous uterine scar
  • fetal heart rate abnormalities at the time of enrollment (bradycardia, tachycardia or prolonged variable decelerations).
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Erich Cosmi MD, PhD, Director of Maternal and Fetal Medicine, Department of Woman and Child Health, University of Padua
ClinicalTrials.gov Identifier: NCT01566331     History of Changes
Other Study ID Numbers: unipd
Study First Received: March 19, 2012
Last Updated: March 26, 2012
Health Authority: BS EN ISO 14155-1:2009; UNI EN ISO 14155-2:2009
Italy: Ministry of Health

Keywords provided by University of Padua:
Safe Delivery
reduction of pain
reduction stage of labor

ClinicalTrials.gov processed this record on July 29, 2014