Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04671680 · ClinicalTrials.gov registry record
CNAP vs IABP in Pregnant Women With Placenta Accreta
A clinical trial, sponsored by Beth Israel Deaconess Medical Center.
- Terminated
- Registry status
- 20
- Enrollment target
NCT04671680: Clinical Trial study, sponsored by Beth Israel Deaconess Medical Center.
NCT04671680 is a clinical trial that was terminated before completion, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04671680 was terminated before completion, sponsored by Beth Israel Deaconess Medical Center.
- TERMINATED
- Registry status
- 20 participants
- Enrollment target
Study Summary
The objective of this study is to investigate a technique to monitor blood pressure in women undergoing cesarean delivery with suspected placenta accreta spectrum. To achieve this objective, the investigators plan to conduct a prospective, observational study with the following aims: Specific Aim 1: Compare concordance between the systolic (SBP), diastolic (DBP), and mean arterial blood pressure (MAP) readings from the continuous non-invasive arterial blood pressure (CNAP) and IABP at several discrete points throughout the procedure Specific Aim 2: Determine the feasibility of using CNAP to aid in decision making by examining the parameters of volume responsiveness and arterial elastance at several discrete points throughout the procedure. The investigators hypothesize that the investigators can obtain similar blood pressure monitoring using CNAP as compared to the gold standard IABP in women undergoing cesarean delivery with suspected placenta accreta.
Primary Outcome
Comparing concordance of systolic blood pressure, mean arterial blood pressure, and diastolic blood pressure readings captured from the continuous non-invasive arterial blood pressure measurements and invasive arterial blood pressure measurements.
Interventions
- DEVICE LiDCO CNAP Monitoring Equipment
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2021-01-15 |
| Est. Completion | 2025-06-01 |
Why NCT04671680 stopped before completion
NCT04671680 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which LiDCO CNAP Monitoring Equipment is the first listed.
NCT04671680 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04671680 about?
NCT04671680 is a clinical study titled "CNAP vs IABP in Pregnant Women With Placenta Accreta". The objective of this study is to investigate a technique to monitor blood pressure in women undergoing cesarean delivery with suspected placenta accreta spectrum. To achieve this objective, the investigators plan to conduct a prospective, observational study with the following aims: Specific Aim 1...
What is the current status of trial NCT04671680?
This trial is currently terminated. The enrollment target is 20 participants. The study started on 2021-01-15. Estimated completion is 2025-06-01.
What interventions are being tested in trial NCT04671680?
The interventions under investigation include: LiDCO CNAP Monitoring Equipment (DEVICE).
Who is sponsoring clinical trial NCT04671680?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
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
- NCT00573339 · 20 participants
Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing
- NCT00692939 · 20 participants · Phase 1
Autologous Stem Cell Transplantation for Crohn's Disease
- NCT00967785 · 20 participants · Phase 1
A Phase I Study of Mozobil in the Treatment of Patients With WHIMS
- NCT01406691 · 20 participants · Phase 4
Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)
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