Clinical Trials Directory

Trials / Completed

CompletedNCT01542151

Effects of Sleep, Fatigue, and Timing of Post-dates Inductions Among Nulliparas

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
University of California, San Francisco · Academic / Other
Sex
Female
Age
14 Years
Healthy volunteers
Not accepted

Summary

This randomized clinical trial will examine if there are any differences between post-dates inductions (inductions after 40 weeks of pregnancy) begun in the morning compared to the evening for first-time mothers. Sleep and fatigue measures will be measured to see if they differ by time of induction. Other measures will include the rate of births within 24 hours of admission, length of labor, use of labor analgesics, and method of delivery.

Detailed description

Randomized clinical trial of first-time pregnant women requiring post-dates induction (induction after 40 weeks gestation). Women will be randomized to a labor induction time in the morning or the evening. On hospital admission once women have signed the study consent, they will complete sleep questionnaires and a fatigue assessment. Fatigue and sleep time assessments will subsequently done by the study subject every 4 hours until women enter active labor. At the onset of active labor, assessments will stop. Labor outcomes and patient satisfaction will be obtained once women deliver.

Conditions

Interventions

TypeNameDescription
OTHERTime of labor inductionAssigned time of labor induction - morning or evening

Timeline

Start date
2011-10-01
Primary completion
2014-11-01
Completion
2014-11-01
First posted
2012-03-02
Last updated
2015-03-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01542151. Inclusion in this directory is not an endorsement.