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

NCT03728517 · ClinicalTrials.gov registry record

Narcotics Inpatient / Outpatient

A clinical trial, sponsored by Indiana University.

Terminated
Registry status
4
Enrollment target

NCT03728517: Clinical Trial study, sponsored by Indiana University.

NCT03728517 is a clinical trial that was terminated before completion, run by Indiana University. The registered enrollment target is 4 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03728517 was terminated before completion, sponsored by Indiana University.

TERMINATED
Registry status
4 participants
Enrollment target

Study Summary

Managing pain in postoperative patients presents challenges in striking a balance between achieving adequate pain control and over-prescribing opioids that have the potential to contribute to the opioid epidemic. There are no clear guidelines informing postoperative opioid prescribing in obstetrics and gynecology. The primary aim for this study are to better understand the factors that impact opioid use for pain management in gynecologic surgery patient after discharge. The second aim is to develop a model that incorporates individual patient baseline measures (e.g. anxiety, fibromyalgia score, inpatient narcotic consumption) to predict the amount of opioids needed following discharge.

Primary Outcome

1. Is opioid consumption during the immediate postoperative recovery phase associated with consumption after discharge? 2. Are variables that are known to be associated with opioid consumption, also associated with opioid consumption after discharge? 3. Are there factors which we can use to predict opioid consumption in postoperative patients?

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2018-08-23
Est. Completion 2019-01-01
Indiana University

890 total trials

Why NCT03728517 stopped before completion

NCT03728517 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 4 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT03728517 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03728517 about?

NCT03728517 is a clinical study titled "Narcotics Inpatient / Outpatient". Managing pain in postoperative patients presents challenges in striking a balance between achieving adequate pain control and over-prescribing opioids that have the potential to contribute to the opioid epidemic. There are no clear guidelines informing postoperative opioid prescribing in obstetrics ...

What is the current status of trial NCT03728517?

This trial is currently terminated. The enrollment target is 4 participants. The study started on 2018-08-23. Estimated completion is 2019-01-01.

Who is sponsoring clinical trial NCT03728517?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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

Source: ClinicalTrials.gov NCT03728517, the US trial registry maintained by the National Library of Medicine. NCT03728517 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.