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NCT03075163 · ClinicalTrials.gov registry record · Phase 4

Post-Operative Therapy for Nausea or Vomiting

A Phase 4 study, sponsored by University of California, Davis.

Terminated
Registry status
Phase 4
Development phase
300
Enrollment target

NCT03075163: Clinical Trial Phase 4 study, sponsored by University of California, Davis.

NCT03075163 is a Phase 4 study that was terminated before completion, run by University of California, Davis. The registered enrollment target is 300 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03075163, a Phase 4 study, was terminated before completion, sponsored by University of California, Davis.

TERMINATED
Registry status
Phase 4
Development phase
300 participants
Enrollment target

Study Summary

This is a single site, prospective, randomized controlled study designed to evaluate the impact of acupressure when used as an initial treatment before rescue medications in the treatment of post-operative nausea and/or vomiting at UCD.

Primary Outcome

Difference in the nausea score before and after treatment. Nausea is scored on a scale from 1 to 10 with 1 being no nausea and 10 being severe nausea with impending vomiting. A greater difference is indicative of a better outcome

Interventions

  • DRUG Ondansetron
  • PROCEDURE Acupressure

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2016-10-18
Est. Completion 2018-12
Phase Phase 4
University of California, Davis

657 total trials

Why NCT03075163 stopped before completion

NCT03075163 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 2 interventions - of which Ondansetron is the first listed.

NCT03075163 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03075163 about?

NCT03075163 is a clinical study titled "Post-Operative Therapy for Nausea or Vomiting". This is a single site, prospective, randomized controlled study designed to evaluate the impact of acupressure when used as an initial treatment before rescue medications in the treatment of post-operative nausea and/or vomiting at UCD.

What is the current status of trial NCT03075163?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 300 participants. The study started on 2016-10-18. Estimated completion is 2018-12.

What interventions are being tested in trial NCT03075163?

The interventions under investigation include: Ondansetron (DRUG), Acupressure (PROCEDURE).

Who is sponsoring clinical trial NCT03075163?

This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03075163's enrollment target sits among peer trials

300 269th of 2000 higher than 1,709 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 NCT03075163, the US trial registry maintained by the National Library of Medicine. NCT03075163 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.