Acupuncture for Promotion of Timely Delivery
Completed · Phase 3
Conditions studied: Delivery, Obstetric
In brief
The purpose of this study of 100 pregnant women is to determine if acupuncture using real needles that puncture the skin, starting at thirty seven weeks three days estimated gestational age (EGA), will increase the percentage of women delivering on or before the estimated date of confinement (EDC = 40 weeks EGA), compared with women treated identically but with placebo needles that do not puncture the skin.
Key facts
- Study ID
- NCT00379327
- Run by
- University of Pennsylvania
- People needed
- 103
- Starts
- 2006-01-01
- Expected to finish
- 2007-08-01
- Last updated by the study team
- 2019-08-22
Who can join
Age: 15 and older, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- A singleton pregnancy in cephalic presentation
- Between 34 and 37 weeks gestation
- Their pregnancy dating (due date) confirmed by at least one first or second trimester ultrasound
- No fetal or maternal contraindications to vaginal delivery
- No contraindication to carry to EDC (40w 0d)
- Have the capacity to understand the requirements of the study
You may not qualify if…
- Without adequate information of dating
- High risk of Cesarean Delivery
- Currently receiving acupuncture outside of study
- Uncertainty of gestational age dating (according to the chart documentation)
Where it is running
- St. Francis Hospital — Wilmington, Delaware, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.