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COMPLETED Phase 2

Nonopioid Analgesia After Rotator Cuff Repair

NCT03818919 · View on ClinicalTrials.gov ↗

Study Summary

This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen

Conditions Studied

Interventions

  • DRUG Acetaminophen
  • DRUG Ketorolac
  • DRUG Celecoxib
  • DRUG Gabapentin
  • DRUG Diazepam

Study Locations (1)

Michigan

  • Health Ford Health System — Detroit

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2019-01-22
Est. Completion 2020-12-31
Phase Phase 2

Sponsor

Henry Ford Health System

171 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03818919

The ClinicalTrials.gov registry entry for NCT03818919 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Henry Ford Health System, which has 171 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Rotator Cuff Tear appearing as the primary indexed condition, and to 5 interventions — of which Acetaminophen is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03818919 reports 1 study location spanning 1 distinct geographic area — top geographies include Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03818919 about?

NCT03818919 is a clinical study titled "Nonopioid Analgesia After Rotator Cuff Repair". This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given sta...

What is the current status of trial NCT03818919?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 70 participants. The study started on 2019-01-22. Estimated completion is 2020-12-31.

What conditions does trial NCT03818919 study?

This clinical trial studies the following conditions: Rotator Cuff Tear. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03818919?

The interventions under investigation include: Acetaminophen (DRUG), Ketorolac (DRUG), Celecoxib (DRUG), Gabapentin (DRUG), Diazepam (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03818919?

This trial is sponsored by Henry Ford Health System, which has 171 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03818919 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial