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RECRUITING NA

Auriculotherapy in the Treatment of Pre-Operative Anxiety

NCT04836936 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to use the validated PROMIS Emotional Distress - Anxiety - Short Form 8a and PROMIS Emotional Distress-Depression-Short Form pre-and post-intervention to establish a superior correlation between the auriculotherapy treatment and the reduction of perioperative anxiety. Subject population will include those having a partial or total nephrectomy for cancer. Drawing the role that auriculotherapy may play in reducing perioperative anxiety related requirement after surgery may also help in reducing the risk of opioid use disorders (OUD) since anxiety has been found to be a major risk factor for OUD in surgical patients. Therefore, this trial will also examine the effect of the auriculotherapy intervention in reducing opioid requirement after surgery.

Conditions Studied

Interventions

  • DEVICE Auriculotherapy cryopuncture device without nitrogen gas
  • DEVICE Auriculotherapy cryopuncture device with nitrogen gas

Study Locations (1)

Pennsylvania

  • UPMC Shadyside Hospital — Pittsburgh

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2021-04-13
Est. Completion 2026-03-30
Phase NA

Sponsor

Jacques E. Chelly

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04836936

The ClinicalTrials.gov registry entry for NCT04836936 describes a study currently listed as recruiting. It is categorized as NA, 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 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Jacques E. Chelly, which has 4 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 Anxiety Preoperative appearing as the primary indexed condition, and to 2 interventions — of which Auriculotherapy cryopuncture device without nitrogen gas 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: NCT04836936 reports 1 study location spanning 1 distinct geographic area — top geographies include Pennsylvania. 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 NCT04836936 about?

NCT04836936 is a clinical study titled "Auriculotherapy in the Treatment of Pre-Operative Anxiety". The goal of this clinical trial is to use the validated PROMIS Emotional Distress - Anxiety - Short Form 8a and PROMIS Emotional Distress-Depression-Short Form pre-and post-intervention to establish a superior correlation between the auriculotherapy treatment and the reduction of perioperative anxie...

What is the current status of trial NCT04836936?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2021-04-13. Estimated completion is 2026-03-30.

What conditions does trial NCT04836936 study?

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

What interventions are being tested in trial NCT04836936?

The interventions under investigation include: Auriculotherapy cryopuncture device without nitrogen gas (DEVICE), Auriculotherapy cryopuncture device with nitrogen gas (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04836936?

This trial is sponsored by Jacques E. Chelly, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04836936 being conducted?

This trial has 1 study location across Pennsylvania. 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