Passive Descent in Obese Nulliparous Gravidae

Not Applicable

• Conditions: Management of the Second Stage of Labor in Obese Nulliparous Women by Either Passive Descent or Immediate Pushing.
• Interventions: Procedure: Pushing; Procedure: Passive Descent

• Registration Number: NCT02080429
• Lead Sponsor: Women and Infants Hospital of Rhode Island

Brief Summary

Obesity rates in reproductive aged women in the United States are rising. It is now universally accepted that obesity is associated with many adverse pregnancy outcomes and post-operative complications following cesarean section. Recent studies have also shown an increased rate of cesarean section in obese women, adding to the already elevated rate of complications and adverse outcomes. Given the increased a priori risk for obese patients, it is vital that the investigators reexamine management practices routinely used for normal weight women in this specific high-risk population. Passive descent has been shown to increase the spontaneous vaginal delivery rate in non-obese women; however, high quality studies have never been performed in obese women. the investigators hypothesize that passive descent could improve the spontaneous vaginal delivery rate in nulliparous, obese women with regional anesthesia. This study will randomize women to passive descent for ninety minutes or active pushing upon entry into the second stage. Further, given that passive descent is widely accepted in the midwifery literature and clinical practice, the investigators anticipate that a high-quality study in the physician literature could increase the dialogue between practitioners and lead to development of best practices in this high-risk population.

Detailed Description

Not available

Study Timeline

• Status Verified: 2014-03
• Study First Submitted: 2014-03-03
• Study First Submitted QC: 2014-03-05
• Last Update Submitted: 2014-03-05
• Study First Posted: 2014-03-06
• Last Update Posted: 2014-03-06
• Primary Completion: 2015-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 540

Inclusion Criteria

• Obese - body mass index (BMI) calculated as weight (kg)/ [height (m2)] greater than or equal to 30 as determined at the time of admission to labor and delivery
• Regional anesthesia
• Nulliparous (defined as no deliveries after 20 weeks gestation)
• Gestational age of 37 0/7 weeks and greater
• Singleton Pregnancy

Exclusion Criteria

• Body mass index (BMI) calculated as weight (kg)/ [height (m2)] less than 30 as determined at the time of admission to labor and delivery
• No regional anesthesia
• Multiparous
• Gestational age of less than 37 0/7 weeks
• Multiple gestations
• Maternal fever prior to second stage
• Severe fetal anomalies (incompatible with life)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Immediate Pushing	Pushing	Patient's will begin to push when they are determined to be completely dilated.
Passive Descent	Passive Descent	Patient's will wait 90 minutes prior to begin pushing

Primary Outcome Measures

Name	Time	Method
Rate of spontaneous vaginal delivery	At delivery

Secondary Outcome Measures

Name	Time	Method
Rate of infections (defined as fever and / or antibiotic initiation)	participants will be followed for the duration of hospital stay, an expected average of 3 days
Rate of Third and Fourth Degree Lacerations	At delivery
Rate of Postpartum Hemorrhage	At delivery
Neonatal Outcomes	At delivery	* admission to NICU; * umbilical cord pH \<7.1

Trial Locations

Locations (1)

Women and Infants Hospital; 🇺🇸 Providence, Rhode Island, United States