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NCT03732469 · ClinicalTrials.gov registry record · Phase 4

Rectal Acetaminophen Use During Oocyte Retrievals to Reduce Post-Operative Opioid Utilization

A Phase 4 study, sponsored by University of South Florida.

Terminated
Registry status
Phase 4
Development phase
4
Enrollment target

NCT03732469: Clinical Trial Phase 4 study, sponsored by University of South Florida.

NCT03732469 is a Phase 4 study that was terminated before completion, run by University of South Florida. The registered enrollment target is 4 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03732469, a Phase 4 study, was terminated before completion, sponsored by University of South Florida.

TERMINATED
Registry status
Phase 4
Development phase
4 participants
Enrollment target

Study Summary

The primary aim of this study is to evaluate the administration of rectal acetaminophen to current and standard anesthesia and analgesia protocol in oocyte retrievals would reduce postoperative utilization of opioids (Tylenol with codeine) in fertility patients.

Primary Outcome

The proportion of prescribed Tylenol with Codeine (Tylenol #3) utilized 72 hours postoperatively will be assessed by telephone encounter. A total of 10 tablets of Tylenol #3 will be prescribed to each participant. Fewer Tylenol #3 used at the end of this time frame would indicate better outcome.

Interventions

  • DRUG Acetaminophen
  • DRUG Propofol
  • DRUG Fentanyl

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2019-11-01
Est. Completion 2021-03-01
Phase Phase 4
University of South Florida

252 total trials

Why NCT03732469 stopped before completion

NCT03732469 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 3 interventions - of which Acetaminophen is the first listed.

NCT03732469 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03732469 about?

NCT03732469 is a clinical study titled "Rectal Acetaminophen Use During Oocyte Retrievals to Reduce Post-Operative Opioid Utilization". The primary aim of this study is to evaluate the administration of rectal acetaminophen to current and standard anesthesia and analgesia protocol in oocyte retrievals would reduce postoperative utilization of opioids (Tylenol with codeine) in fertility patients.

What is the current status of trial NCT03732469?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 4 participants. The study started on 2019-11-01. Estimated completion is 2021-03-01.

What interventions are being tested in trial NCT03732469?

The interventions under investigation include: Acetaminophen (DRUG), Propofol (DRUG), Fentanyl (DRUG).

Who is sponsoring clinical trial NCT03732469?

This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03732469's enrollment target sits among peer trials

4 1994th of 2000 higher than 6 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

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Source: ClinicalTrials.gov NCT03732469, the US trial registry maintained by the National Library of Medicine. NCT03732469 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.