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COMPLETED Phase 4

Optimal Timing of Intercostal Nerve Blocks During Video-Assisted Thoracic Surgeries

NCT02980835 · View on ClinicalTrials.gov ↗

Study Summary

Intercostal nerve block, performed under the guidance of videoscope, is a part of standard anesthesia procedures for patients receiving Video-Assisted Thoracic Surgeries. In this double-blind, prospective, multi-center, randomized, controlled clinical trial the investigators aim to compare preemptive versus post-closure intercostal injection of ropivacaine in controlling post-video-assisted thoracotomy pain.

Interventions

  • DRUG Dexamethasone
  • DRUG Epinephrine
  • DRUG Normal Saline
  • DRUG Ropivacaine

Study Locations (1)

New York

  • VA Western New York Healthcare System — Buffalo

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2016-09-28
Est. Completion 2022-03-30
Phase Phase 4

Sponsor

University at Buffalo

11 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02980835

The ClinicalTrials.gov registry entry for NCT02980835 describes a study currently listed as completed. It is categorized as Phase 4, 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 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University at Buffalo, which has 11 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Video-Assisted Thoracic Surgery appearing as the primary indexed condition, and to 4 interventions — of which Dexamethasone 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: NCT02980835 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. 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 NCT02980835 about?

NCT02980835 is a clinical study titled "Optimal Timing of Intercostal Nerve Blocks During Video-Assisted Thoracic Surgeries". Intercostal nerve block, performed under the guidance of videoscope, is a part of standard anesthesia procedures for patients receiving Video-Assisted Thoracic Surgeries. In this double-blind, prospective, multi-center, randomized, controlled clinical trial the investigators aim to compare preemptiv...

What is the current status of trial NCT02980835?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 36 participants. The study started on 2016-09-28. Estimated completion is 2022-03-30.

What conditions does trial NCT02980835 study?

This clinical trial studies the following conditions: Video-Assisted Thoracic Surgery, Video-Assisted Thoracoscopic Surgery. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02980835?

The interventions under investigation include: Dexamethasone (DRUG), Epinephrine (DRUG), Normal Saline (DRUG), Ropivacaine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02980835?

This trial is sponsored by University at Buffalo, which has 11 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02980835 being conducted?

This trial has 1 study location across New York. 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