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NCT05805423 · ClinicalTrials.gov registry record · NA
ENDOblock: Bilateral Superficial Cervical Blocks With Local Wound Infiltration in Thyroid Surgery
A NA study of Opioid Use and Post Operative Pain, sponsored by University of California, Davis.
- Active
- Registry status
- NA
- Development phase
- 74
- Enrollment target
- 1
- Study location
NCT05805423 is a NA study of Opioid Use and Post Operative Pain that is active but no longer recruiting, run by University of California, Davis. The registered enrollment target is 74 participants, below the 148,259-participant average among 105 other Opioid Use trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05805423, a NA study of Opioid Use and Post Operative Pain, is active but no longer recruiting, sponsored by University of California, Davis.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 74 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a single center, prospective, double-blinded randomized controlled trial comparing the efficacy of bilateral superficial cervical plexus blocks (BSCPB) with local wound infiltration vs placebo with local wound infiltration in reducing thyroid surgery postoperative pain. Primary outcomes assessed are post operative pain, quality of life/recovery, post operative nausea/vomiting and opioid use.
Conditions Studied
Interventions
- PROCEDURE bilateral superficial cervical plexus blocks and local wound infiltration
- PROCEDURE placebo injection and local wound infiltration
Study Locations (1)
California
- UC Davis Medical Center - Sacramento
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2023-04-17 |
| Est. Completion | 2026-04 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05805423
The ClinicalTrials.gov registry entry for NCT05805423 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 74 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 148,259-participant average among 105 other Opioid Use trials with a reported enrollment target (100% lower). The listed sponsor is University of California, Davis, which has 657 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Opioid Use appearing as the primary indexed condition, and to 2 interventions - of which bilateral superficial cervical plexus blocks and local wound infiltration is the first listed.
NCT05805423 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT05805423 about?
NCT05805423 is a clinical study titled "ENDOblock: Bilateral Superficial Cervical Blocks With Local Wound Infiltration in Thyroid Surgery". This is a single center, prospective, double-blinded randomized controlled trial comparing the efficacy of bilateral superficial cervical plexus blocks (BSCPB) with local wound infiltration vs placebo with local wound infiltration in reducing thyroid surgery postoperative pain. Primary outcomes asse...
What is the current status of trial NCT05805423?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 74 participants. The study started on 2023-04-17. Estimated completion is 2026-04.
What conditions does trial NCT05805423 study?
This clinical trial studies the following conditions: Opioid Use, Post Operative Pain, Nausea and Vomiting, Postoperative.
What interventions are being tested in trial NCT05805423?
The interventions under investigation include: bilateral superficial cervical plexus blocks and local wound infiltration (PROCEDURE), placebo injection and local wound infiltration (PROCEDURE).
Who is sponsoring clinical trial NCT05805423?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05805423 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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