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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 Postoperative Pain and Opioid Use, sponsored by University of California, Davis.
- Active
- Registry status
- NA
- Development phase
- 74
- Enrollment target
- 1
- Study location
NCT05805423: Active NA study of Postoperative Pain and Opioid Use, sponsored by University of California, Davis.
NCT05805423 is a NA study of Postoperative Pain and Opioid Use that is active but no longer recruiting, run by University of California, Davis. The registered enrollment target is 74 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (68% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05805423, a NA study of Postoperative Pain and Opioid Use, 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.
Primary Outcome
Neck pain intensity will be quantified using the numeric rating scale (visual analog score 0-10, VAS). Higher scores mean more pain. Lower scores are a better outcome
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 |
What the registry record for NCT05805423 still lists
NCT05805423 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (68% lower).
The record links to 3 conditions, with Postoperative Pain 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 a single indexed study location in 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: Postoperative Pain, Opioid Use, 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.
Learn More About Clinical Trials
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Where NCT05805423's enrollment target sits among peer trials
74 81st of 120 higher than 40 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain 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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