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NCT07434583 · ClinicalTrials.gov registry record · NA
Force Sensor Study
A NA study of Postoperative Pain and Laryngeal Disease, sponsored by University of California, San Francisco.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT07434583: Recruiting NA study of Postoperative Pain and Laryngeal Disease, sponsored by University of California, San Francisco.
NCT07434583 is a NA study of Postoperative Pain and Laryngeal Disease that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 100 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07434583, a NA study of Postoperative Pain and Laryngeal Disease, is actively recruiting participants, sponsored by University of California, San Francisco.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
This research is to understand more about the forces that are involved on the tongue and other oropharyngeal structures during laryngeal surgery. This information will be used to determine if these forces can affect outcomes (pain, numbness, taste, etc) and whether factors such as procedure type, surgeon experience (i.e. resident, fellow, attending), and choice of surgical equipment affect these forces. This information may be used to reduce these forces and prevent these issues from happening during certain laryngeal surgeries. For the first 50 patients, force measurements will be taken and correlated to outcome measures . Surgeons will be blinded to the force measurements intra-operatively. For the next 50 patients, surgeons will be given force measurements in real-time intra-operatively allowing adjustments to be made. The impact of this adjustment on outcomes will be determined.
Primary Outcome
The SF-MPQ includes the following components: 15 descriptors: * 11 sensory, each rated 0=none, 1=mild, 2=moderate, 3=severe * 4 affective , each rated 0=none, 1=mild, 2=moderate, 3=severe. A Present Pain Intensity (PPI) scale (0=No Pain, 1=Mild, 2=Discomforting, 3=Distressing, 4=Horrible, 5=Excruciating) Visual Analogue Scale of average pain (VAS, 0-10 cm) - higher score is worse pain
Conditions Studied
Interventions
- PROCEDURE Direct laryngoscopy force modulation
- PROCEDURE Direct laryngoscopy without force modulation
Study Locations (1)
California
- University of California San Francisco - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2026-01-02 |
| Est. Completion | 2027-01-31 |
| Phase | NA |
What NCT07434583 shows while recruiting
NCT07434583 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (57% lower).
The record links to 3 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Direct laryngoscopy force modulation is the first listed.
NCT07434583 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT07434583 about?
NCT07434583 is a clinical study titled "Force Sensor Study". This research is to understand more about the forces that are involved on the tongue and other oropharyngeal structures during laryngeal surgery. This information will be used to determine if these forces can affect outcomes (pain, numbness, taste, etc) and whether factors such as procedure type, su...
What is the current status of trial NCT07434583?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2026-01-02. Estimated completion is 2027-01-31.
What conditions does trial NCT07434583 study?
This clinical trial studies the following conditions: Postoperative Pain, Laryngeal Disease, Tongue Injury.
What interventions are being tested in trial NCT07434583?
The interventions under investigation include: Direct laryngoscopy force modulation (PROCEDURE), Direct laryngoscopy without force modulation (PROCEDURE).
Who is sponsoring clinical trial NCT07434583?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07434583 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
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07434583's enrollment target sits among peer trials
100 55th of 120 higher than 59 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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