Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01190605 · ClinicalTrials.gov registry record

Evaluating Factors That Impact Loss to Follow-up Among Postpartum HIV-infected Women in Mississippi

A clinical trial of HIV, sponsored by University of Mississippi Medical Center.

Completed
Registry status
53
Enrollment target
1
Study location

NCT01190605: Completed study of HIV, sponsored by University of Mississippi Medical Center.

NCT01190605 is a study of HIV that has completed, run by University of Mississippi Medical Center. The registered enrollment target is 53 participants, below the 440-participant average among 303 other HIV 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.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01190605, a study of HIV, has completed, sponsored by University of Mississippi Medical Center.

COMPLETED
Registry status
53 participants
Enrollment target
1
Study location

Study Summary

Women with HIV infection in Mississippi who are pregnant or who have had their baby in the past year can agree to fill out a questionnaire about what helps or hurts return to care for HIV infection after having a baby. The combined results should show the most common things that keep women from getting care for HIV infection after having a baby. This will help design another study in order to help more women get into care for HIV infection after having a baby.

Primary Outcome

retrospective chart review for documentation of visit attendance

Conditions Studied

Study Locations (1)

Mississippi

  • University of Mississippi Medical Center - Jackson

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2010-07
Est. Completion 2013-07

What the finished NCT01190605 record still lists

NCT01190605 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 440-participant average among 303 other HIV trials with a reported enrollment target (88% lower).

The record links to 1 condition, with HIV appearing as the primary indexed condition, and to 0 interventions.

NCT01190605 reports a single indexed study location in Mississippi.

Frequently Asked Questions

What is clinical trial NCT01190605 about?

NCT01190605 is a clinical study titled "Evaluating Factors That Impact Loss to Follow-up Among Postpartum HIV-infected Women in Mississippi". Women with HIV infection in Mississippi who are pregnant or who have had their baby in the past year can agree to fill out a questionnaire about what helps or hurts return to care for HIV infection after having a baby. The combined results should show the most common things that keep women from gett...

What is the current status of trial NCT01190605?

This trial is currently completed. The enrollment target is 53 participants. The study started on 2010-07. Estimated completion is 2013-07.

What conditions does trial NCT01190605 study?

This clinical trial studies the following conditions: HIV.

Who is sponsoring clinical trial NCT01190605?

This trial is sponsored by University of Mississippi Medical Center, which has 96 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01190605 being conducted?

This trial has 1 study location across Mississippi. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for HIV

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 NCT01190605's enrollment target sits among peer trials

53 214th of 303 higher than 88 of 303 other HIV trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other HIV 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

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

  • NCT04177004 · 53 participants · Phase 1

    Human Lysozyme Goat Milk for the Prevention of Graft Versus Host Disease in Patients With Blood Cancer Undergoing a Donor Stem Cell Transplant

  • NCT04199741 · 53 participants · Phase 1

    PET/CT Imaging of Small Cell Lung Cancer Using 89Zr-DFO-SC16.56

  • NCT04835129 · 53 participants · Phase 2

    Isatuximab, Pomalidomide, Elotuzumab and Dexamethasone in Relapsed and/or Refractory Multiple Myeloma

  • NCT04913805 · 53 participants · Phase 2

    Matching Perfusion and Metabolic Activity in HFpEF

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

Source: ClinicalTrials.gov NCT01190605, the US trial registry maintained by the National Library of Medicine. NCT01190605 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.