Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04756089 · ClinicalTrials.gov registry record · NA
Stimulation Therapy for Inducing Mothers
A NA study of Labor Pain and Induced; Birth, sponsored by Yale University.
- Completed
- Registry status
- NA
- Development phase
- 24
- Enrollment target
- 1
- Study location
NCT04756089: Completed NA study of Labor Pain and Induced; Birth, sponsored by Yale University.
NCT04756089 is a NA study of Labor Pain and Induced; Birth that has completed, run by Yale University. The registered enrollment target is 24 participants, below the 202-participant average among 14 other Labor Pain trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04756089, a NA study of Labor Pain and Induced; Birth, has completed, sponsored by Yale University.
- COMPLETED
- Registry status
- NA
- Development phase
- 24 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a pilot feasibility and acceptability study of a randomized clinical trial of pregnant women at 36 weeks of gestation and greater randomized to one of two arms at Yale New Haven Hospital: (1) Breast stimulation by hand or with an electronic breast pump (intervention) compared to (2) Exogenous oxytocin intravenous infusion (current standard of care, control). The pilot study will be randomized since one of the goals is to evaluate whether the idea of randomization would be acceptable to patients.
Primary Outcome
Determine the rate of eligible women who consent and enroll in the study among eligible women who are approached by research study staff.
Conditions Studied
Interventions
- DEVICE Electronic breast pump
- OTHER Exogenous oxytocin intravenous infusion
Study Locations (1)
Connecticut
- Yale New Haven Hospital - New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2021-03-13 |
| Est. Completion | 2021-06-23 |
| Phase | NA |
What the finished NCT04756089 record still lists
NCT04756089 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 202-participant average among 14 other Labor Pain trials with a reported enrollment target (88% lower).
The record links to 5 conditions, with Labor Pain appearing as the primary indexed condition, and to 2 interventions - of which Electronic breast pump is the first listed.
NCT04756089 reports a single indexed study location in Connecticut.
Frequently Asked Questions
What is clinical trial NCT04756089 about?
NCT04756089 is a clinical study titled "Stimulation Therapy for Inducing Mothers". This is a pilot feasibility and acceptability study of a randomized clinical trial of pregnant women at 36 weeks of gestation and greater randomized to one of two arms at Yale New Haven Hospital: (1) Breast stimulation by hand or with an electronic breast pump (intervention) compared to (2) Exogenou...
What is the current status of trial NCT04756089?
This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2021-03-13. Estimated completion is 2021-06-23.
What conditions does trial NCT04756089 study?
This clinical trial studies the following conditions: Labor Pain, Induced; Birth, Labor Long, Breast Pumping, Lactation Induced.
What interventions are being tested in trial NCT04756089?
The interventions under investigation include: Electronic breast pump (DEVICE), Exogenous oxytocin intravenous infusion (OTHER).
Who is sponsoring clinical trial NCT04756089?
This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04756089 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Labor Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT04756089's enrollment target sits among peer trials
24 13th of 14 higher than 2 of 14 other Labor Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Labor Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
CSE v. Epidural for Postpartum Depression
COMPLETED · NA
-
Virtual Reality Compared to Nitrous Oxide for Labor Analgesia
COMPLETED · NA
-
Use of Ultrasound Guidance to Assist With Labor Epidural Placement in Patients With a BMI ≥40
COMPLETED · NA
-
Impact of Dural Puncture Epidural Versus Traditional Lumbar Epidural on Onset of Labor Analgesia
COMPLETED · NA
-
Best Beginnings for Babies Birth Sister Program Evaluation
COMPLETED · NA
-
The Stimulation To Induce Mothers Study
RECRUITING · Phase 4
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02331979 · 24 participants · NA
Improving Bladder Function in SCI by Neuromodulation
- NCT03096197 · 24 participants · NA
Exoskeleton and Spinal Cord Stimulation for SCI
- NCT03223922 · 24 participants · NA
Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases
- NCT03326921 · 24 participants · Phase 1
HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI