Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01063244 · ClinicalTrials.gov registry record · Phase 3
Comparison of Foley Balloon With or Without Traction for the Cervical Ripening
A Phase 3 study of Pregnancy, sponsored by St. Luke's Hospital, Pennsylvania.
- Completed
- Registry status
- Phase 3
- Development phase
- 65
- Enrollment target
- 1
- Study location
NCT01063244: Completed Phase 3 study of Pregnancy, sponsored by St. Luke's Hospital, Pennsylvania.
NCT01063244 is a Phase 3 study of Pregnancy that has completed, run by St. Luke's Hospital, Pennsylvania. The registered enrollment target is 65 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01063244, a Phase 3 study of Pregnancy, has completed, sponsored by St. Luke's Hospital, Pennsylvania.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 65 participants
- Enrollment target
- 1
- Study location
Study Summary
We will compare the use of foley bulb catheters placed in the cervix for ripening of the cervix for labor induction,.
Conditions Studied
Interventions
- DEVICE foley balloon only
- DEVICE foley balloon with weight attached
Study Locations (1)
Pennsylvania
- St Luke's Hosptial & Health Network - Bethlehem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2009-01 |
| Est. Completion | 2012-01 |
| Phase | Phase 3 |
What the finished NCT01063244 record still lists
NCT01063244 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (93% lower).
The record links to 1 condition, with Pregnancy appearing as the primary indexed condition, and to 2 interventions - of which foley balloon only is the first listed.
NCT01063244 reports a single indexed study location in Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01063244 about?
NCT01063244 is a clinical study titled "Comparison of Foley Balloon With or Without Traction for the Cervical Ripening". We will compare the use of foley bulb catheters placed in the cervix for ripening of the cervix for labor induction,.
What is the current status of trial NCT01063244?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 65 participants. The study started on 2009-01. Estimated completion is 2012-01.
What conditions does trial NCT01063244 study?
This clinical trial studies the following conditions: Pregnancy.
What interventions are being tested in trial NCT01063244?
The interventions under investigation include: foley balloon only (DEVICE), foley balloon with weight attached (DEVICE).
Who is sponsoring clinical trial NCT01063244?
This trial is sponsored by St. Luke's Hospital, Pennsylvania, which has 10 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01063244 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pregnancy
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 NCT01063244's enrollment target sits among peer trials
65 139th of 191 higher than 52 of 191 other Pregnancy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pregnancy 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
-
Different Medications to Induce Labor
RECRUITING · Phase 3
-
Ropivacaine and Fentanyl for Labor Epidural Initiation
RECRUITING · Phase 3
-
Intravenous Versus Oral Iron for Treating Iron-Deficiency Anemia in Pregnancy
RECRUITING · Phase 3
-
A Phase III Randomized, Double-Blind, Controlled Study of the Use of Anti-HIV Immune Serum Globulin (HIVIG) for the Prevention of Maternal-Fetal HIV Transmission in Pregnant Women and Newborns Receiving Zidovudine (AZT)
COMPLETED · Phase 3
-
The Safety and Effectiveness of Zidovudine in HIV-Infected Pregnant Women and Their Infants
COMPLETED · Phase 3
-
Induction With Misoprostol: Oral Mucosa Versus Vaginal Epithelium (IMPROVE)
COMPLETED · Phase 3
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
- NCT03366116 · 65 participants · Phase 1
5-aza-4'-Thio-2'-Deoxycytidine (Aza-TdC) in People With Advanced Solid Tumors
- NCT03603730 · 65 participants · NA
Vagal Nerve Stimulation for Functional Dyspepsia and Gastroparesis
- NCT03796559 · 65 participants · NA
Magseed Enabled Long-Term Localization of Axillary Lymph Nodes
- NCT03993106 · 65 participants · Phase 2
A Study of sEphB4-HSA in Kaposi Sarcoma
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia