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Passive Descent in Obese Nulliparous Gravidae

Women and Infants Hospital of Rhode Island logo

Women and Infants Hospital of Rhode Island

Status

Unknown

Conditions

Management of the Second Stage of Labor in Obese Nulliparous Women by Either Passive Descent or Immediate Pushing.

Treatments

Procedure: Passive Descent
Procedure: Pushing

Study type

Interventional

Funder types

Other

Identifiers

NCT02080429
WIHRI-PD

Details and patient eligibility

About

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.

Enrollment

540 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

540 participants in 2 patient groups

Immediate Pushing
Active Comparator group
Description:
Patient's will begin to push when they are determined to be completely dilated.
Treatment:
Procedure: Pushing
Passive Descent
Experimental group
Description:
Patient's will wait 90 minutes prior to begin pushing
Treatment:
Procedure: Passive Descent

Trial contacts and locations

1

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Central trial contact

Alisse Hauspurg, MD

Data sourced from clinicaltrials.gov

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