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NCT06218355 · ClinicalTrials.gov registry record · NA

IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine

A NA study of Postpartum Complication, sponsored by University of Texas Southwestern Medical Center.

Recruiting
Registry status
NA
Development phase
3,500
Enrollment target
2
Study locations

NCT06218355: Recruiting NA study of Postpartum Complication, sponsored by University of Texas Southwestern Medical Center.

NCT06218355 is a NA study of Postpartum Complication that is actively recruiting participants, run by University of Texas Southwestern Medical Center. The registered enrollment target is 3,500 participants, above the 1,643-participant average among 3 other Postpartum Complication trials with a reported enrollment target (113% higher). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06218355, a NA study of Postpartum Complication, is actively recruiting participants, sponsored by University of Texas Southwestern Medical Center.

RECRUITING
Registry status
NA
Development phase
3,500 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to compare two complex, multi-component evidence-based postpartum interventions in underserved populations of lower socioeconomic status in an effort to reduce maternal morbidity and mortality.

Primary Outcome

Time to diagnosis and treatment of postpartum complications including hypertension, wound infection, and venous thromboembolism, measured in days. Lower value is considered better, representing timely care.

Conditions Studied

Interventions

  • OTHER Intensive Education
  • OTHER Enhanced Virtual Care

Study Locations (2)

Georgia

  • Emory University School of Medicine - Atlanta

Texas

  • University of Texas Southwestern Medical Center - Dallas

Trial Details

FieldValue
Enrollment Target 3,500 participants
Start Date 2024-03-01
Est. Completion 2028-09-01
Phase NA

What NCT06218355 shows while recruiting

NCT06218355 is an interventional study that assigns participants to a tested intervention. Its 3,500 participants enrollment target places it among the larger protocols in the corpus, above the 1,643-participant average among 3 other Postpartum Complication trials with a reported enrollment target (113% higher).

The record links to 1 condition, with Postpartum Complication appearing as the primary indexed condition, and to 2 interventions - of which Intensive Education is the first listed.

NCT06218355 reports a single indexed study location in Georgia, Texas.

Frequently Asked Questions

What is clinical trial NCT06218355 about?

NCT06218355 is a clinical study titled "IMPACT: Improving Maternal Postpartum Access to Care Through Telemedicine". The purpose of this study is to compare two complex, multi-component evidence-based postpartum interventions in underserved populations of lower socioeconomic status in an effort to reduce maternal morbidity and mortality.

What is the current status of trial NCT06218355?

This trial is currently recruiting. It is a NA study. The enrollment target is 3,500 participants. The study started on 2024-03-01. Estimated completion is 2028-09-01.

What conditions does trial NCT06218355 study?

This clinical trial studies the following conditions: Postpartum Complication.

What interventions are being tested in trial NCT06218355?

The interventions under investigation include: Intensive Education (OTHER), Enhanced Virtual Care (OTHER).

Who is sponsoring clinical trial NCT06218355?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06218355 being conducted?

This trial has 2 study locations across Georgia, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06218355, the US trial registry maintained by the National Library of Medicine. NCT06218355 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.