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NCT02724033 · ClinicalTrials.gov registry record · Phase 4
Comparative Study of Superficial Cervical Plexus Block and Nerve of Arnold Block and Incidence of PONV for Inner Ear Surgery
A Phase 4 study, sponsored by Indiana University.
- Terminated
- Registry status
- Phase 4
- Development phase
- 37
- Enrollment target
NCT02724033 is a Phase 4 study that was terminated before completion, run by Indiana University. The registered enrollment target is 37 participants.
The verdict
NCT02724033, a Phase 4 study, was terminated before completion, sponsored by Indiana University.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 37 participants
- Enrollment target
Study Summary
The investigators would like to compare the therapeutic and cost effectiveness of established therapies for postoperative nausea and vomiting to regional nerve blocks of the head and neck area an intervention known for analgesia but for which the antiemetic effects hasn't been entirely explored. The rational is based on the knowledge of the anatomical innervation of the inner ear and the role of the parasympathetic nervous system in the emetic act. A lot of focus has been given on its counterpart the sympathetic nervous system and its role in painful conditions. The investigators believe that the nerve blockade of the parasympathetic innervation can have some beneficial effect in the post-surgical patient.
Interventions
- DRUG Antiemetic
- PROCEDURE regional nerve block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2014-05 |
| Est. Completion | 2018-09 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02724033
The ClinicalTrials.gov registry entry for NCT02724033 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Antiemetic is the first listed.
NCT02724033 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02724033 about?
NCT02724033 is a clinical study titled "Comparative Study of Superficial Cervical Plexus Block and Nerve of Arnold Block and Incidence of PONV for Inner Ear Surgery". The investigators would like to compare the therapeutic and cost effectiveness of established therapies for postoperative nausea and vomiting to regional nerve blocks of the head and neck area an intervention known for analgesia but for which the antiemetic effects hasn't been entirely explored. Th...
What is the current status of trial NCT02724033?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 37 participants. The study started on 2014-05. Estimated completion is 2018-09.
What interventions are being tested in trial NCT02724033?
The interventions under investigation include: Antiemetic (DRUG), regional nerve block (PROCEDURE).
Who is sponsoring clinical trial NCT02724033?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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