Mouth Guard Use in the Second Stage of Labor

Sponsor
Christiana Care Health Services (Other)
Overall Status
Completed
CT.gov ID
NCT03520530
Collaborator
(none)
154
1
2
18.8
8.2

Study Details

Study Description

Brief Summary

Shortening the second stage of labor, the time spent pushing the baby out, is important for positive mother and infant's outcomes. Lack of progress of labor for any reason is the most common reason for cesarean section in women having their first baby and the second most common reason for cesarean section in women who have already had a baby. In 2014, a large study done across the United States showed increases in complications in both mother and infant when pushing was prolonged, including uterine infection, postpartum hemorrhage, more extensive vaginal tearing, shoulder dystocia, 5 minute Apgar score less than 4, infant admission to Neonatal Intensive Care Unit and neonatal infections. Therefore, the challenge is to consider alternative practices in order to maximize a mother's chance of a vaginal delivery and minimize these associated risks to both mother and baby.

Mouth guards are used primarily in contact sports, and have been demonstrated to reduce or prevent injury to the teeth. Additionally, it has been proposed that wearing a mouth guard increases the strength of different muscle groups. A recent randomized controlled pilot study including women with their first pregnancy using a dental support device (DSD) during the second stage of labor evaluated the length of the second stage and outcomes. They found a significant decrease of 38% in the length of pushing time in the group that used a DSD. Additionally, there was a decreased rate of cesarean section in this group, however a p-value was not reported. This study only included 64 patients. A second, larger trial did not find a significant difference in pushing time, however the rate of interventions such as a vacuum or forceps-assisted vaginal delivery and cesarean section were much higher in the control group due to prolonged pushing. The results of the second study are contradictory in nature, yet the researchers do not provide hypotheses into why this may be.

It is clear from the previously mentioned studies that further research is needed. Our hypothesis is that using such a device would help women to push more effectively during the second stage of labor thus shortening the time needed to push the baby out and increasing the rate of vaginal delivery. The purpose of this study is to determine whether wearing a mouth guard in the second stage of labor affects the length of the second stage of labor and improves mother & infant outcomes.

Condition or Disease Intervention/Treatment Phase
  • Device: Mouth Guard
N/A

Detailed Description

Optimizing the second stage of labor is important for positive maternal and neonatal outcomes. Dystocia of labor refers to a lack of progress of labor for any reason, and it is the most common indication for cesarean delivery in nulliparous women and the second most common indication for cesarean delivery in multiparous women. In 2014, a large US multicenter cohort study showed increases in maternal and neonatal morbidities when the second stage was prolonged, including chorioamnionitis, postpartum hemorrhage, 3rd and 4th degree perineal laceration, shoulder dystocia, 5 minute Apgar score less than 4, neonatal admission to NICU and neonatal sepsis. Therefore, clinicians are challenged to consider alternative practices in order to maximize a mother's chance of a normal delivery and minimize these associated risks to both mother and baby.

Mouth guards are used primarily in contact sports, and have been demonstrated to reduce or prevent injury to the teeth. Most commonly made of synthetic polymers, mouth guards function as a shock-absorber. Even among sports medicine literature, there is a call for more research into use and education about protective gear. Previous studies have shown that wearing a mouth guard increases the isometric strength of different muscle groups. Recent studies have begun to explore whether wearing a similar style mouth guard will shorten the duration of the second stage of labor. A recent randomized controlled pilot study including nulliparous women using a dental support device (DSD) during the second stage evaluated the length of the second stage and outcome thereof. They defined the second stage of labor as the time between complete cervical dilation and fetal expulsion. They found a significant decrease of 38% in the length of the second stage in the group that used a DSD. Additionally, there was a decreased rate of cesarean section in this group, however a p-value was not reported. This study only included 64 patients. A second, larger trial also looking at nulliparous women did not find a significant difference in length of second stage of labor however the rate of obstetrical interventions such as operative vaginal delivery and cesarean section were much higher in the control group due to prolonged second stage of labor. Though the results of the second study are contradictory in nature, the researchers do not provide hypotheses into why this may be.

Our hypothesis is that using such a device would help women to push more effectively during the second stage of labor thus shortening the second stage and increasing the rate of spontaneous vaginal deliveries that do not require operative intervention. Developing a way to shorten the second stage of labor and reduce the number of cesarean sections or instrumental deliveries could reduce the morbidity of mothers and their infants and decrease health care spending.

Study Design

Study Type:
Interventional
Actual Enrollment :
154 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This will be a randomized controlled trial in which patients who make it to the second stage of labor will be randomized to wear a mouth guard while pushing during the second stage of labor or continue through the second stage of labor without a mouth guard. They will be randomized in a 1:1 fashion using RedCap.This will be a randomized controlled trial in which patients who make it to the second stage of labor will be randomized to wear a mouth guard while pushing during the second stage of labor or continue through the second stage of labor without a mouth guard. They will be randomized in a 1:1 fashion using RedCap.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Mouth Guard Use in the Second Stage of Labor: A Randomized Controlled Trial
Actual Study Start Date :
May 9, 2018
Actual Primary Completion Date :
Dec 1, 2019
Actual Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mouth Guard

Patients will push in the second stage of labor without use of mouth guard

Device: Mouth Guard
Patient will wear mouth guard while pushing in the second stage of labor

No Intervention: Control

Patients will push in the second stage of labor without use of mouth guard

Outcome Measures

Primary Outcome Measures

  1. Time of Second Stage of Labor [Time from full cervical dilation (10cm) to delivery of the fetal head, approximately 2 hours]

    Time in minutes

Secondary Outcome Measures

  1. Mode of Delivery [From time of randomization until delivery, up to one week]

    Spontaneous vaginal delivery, assisted vaginal delivery, cesarean section

  2. Instrumental Delivery [From time of randomization until delivery, up to one week]

    Type of instrument used in assisting delivery

  3. Patient Satisfaction [From time of randomization until delivery, up to one week]

    Patient satisfaction with device as measured by survey

  4. Perineal Laceration [From time of randomization until delivery, up to one week]

    Degree of perineal laceration with vaginal delivery

  5. Apgar Score [From 0 to 10 minutes after delivery]

    Apgar scores of infants at 1, 5, and 10 minutes

  6. Percentage of Time Spent Using Device [From time of randomization until delivery, up to one week]

    Provider will estimate percentage of second stage that patient used device

  7. Neonatal ICU Admission Rate [From time of randomization until delivery, up to one week]

    Number of infants admitted to the NICU

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 55 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Nulliparous women

  • Age 18-55

  • Presenting for delivery at Christiana Care Health Services

  • Singleton pregnancy

  • Cephalic pregnancy

  • Term pregnancy

Exclusion Criteria:
  • Multiple gestation

  • Known uterine anomalies, excluding resected uterine septums and fibroids

  • Estimated fetal weight less than 10th% for gestation age with abnormal umbilical dopplers

  • Estimated fetal weight less than the 5th percentile

  • History of cardiac disease requiring assisted second stage of labor

  • Oral implants, braces or active dental infection precluding mouth guard use

  • Preeclampsia with severe features treated with magnesium sulfate

  • History of shoulder dystocia

  • History of myomectomy

  • Maternal history of myasthenia gravis

  • Maternal history of sleep apnea with home CPAP use

  • Category III fetal heart tracing

  • Active vaginal bleeding consistent with placental abruption

  • Diagnosis of chorioamnionitis prior to start of second stage of labor

  • Participation in another interventional research study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Christiana Care Health System Newark Delaware United States 19713

Sponsors and Collaborators

  • Christiana Care Health Services

Investigators

  • Principal Investigator: Elizabeth Shy, MD, Christiana Care Health Services

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Christiana Care Health Services
ClinicalTrials.gov Identifier:
NCT03520530
Other Study ID Numbers:
  • 37133
First Posted:
May 9, 2018
Last Update Posted:
Aug 4, 2020
Last Verified:
Jul 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Christiana Care Health Services
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 4, 2020