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NCT05895383 · ClinicalTrials.gov registry record · Phase 4
Self-Adjusted Nitrous Oxide: A Feasibility Study in the Setting of Vasectomy
A Phase 4 study of Procedural Pain and Procedural Anxiety, sponsored by Beth Israel Deaconess Medical Center.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 35
- Enrollment target
- 1
- Study location
NCT05895383: Recruiting Phase 4 study of Procedural Pain and Procedural Anxiety, sponsored by Beth Israel Deaconess Medical Center.
NCT05895383 is a Phase 4 study of Procedural Pain and Procedural Anxiety that is actively recruiting participants, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 35 participants, below the 57-participant average among 9 other Procedural Pain trials with a reported enrollment target (39% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05895383, a Phase 4 study of Procedural Pain and Procedural Anxiety, is actively recruiting participants, sponsored by Beth Israel Deaconess Medical Center.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 35 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is being done to see if nitrous oxide during vasectomy decreases pain and anxiety, and also assess whether patients have better satisfaction when they control their own level of nitrous oxide during the procedure. If we find that patients experience less pain or anxiety with nitrous oxide, it could be suggested that self-adjusted nitrous oxide (SANO) may be a useful tool for improving experience of care during vasectomy.
Primary Outcome
Level of pain experienced during vasectomy as measured by the Visual Analog Scale for Pain (VAS-P; range: 0 no pain - 10 worst pain).
Conditions Studied
Interventions
- DRUG Nitrous oxide
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2023-05-24 |
| Est. Completion | 2027-01-30 |
| Phase | Phase 4 |
What NCT05895383 shows while recruiting
NCT05895383 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 57-participant average among 9 other Procedural Pain trials with a reported enrollment target (39% lower).
The record links to 3 conditions, with Procedural Pain appearing as the primary indexed condition, and to 1 intervention - of which Nitrous oxide is the first listed.
NCT05895383 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT05895383 about?
NCT05895383 is a clinical study titled "Self-Adjusted Nitrous Oxide: A Feasibility Study in the Setting of Vasectomy". This study is being done to see if nitrous oxide during vasectomy decreases pain and anxiety, and also assess whether patients have better satisfaction when they control their own level of nitrous oxide during the procedure. If we find that patients experience less pain or anxiety with nitrous oxide...
What is the current status of trial NCT05895383?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 35 participants. The study started on 2023-05-24. Estimated completion is 2027-01-30.
What conditions does trial NCT05895383 study?
This clinical trial studies the following conditions: Procedural Pain, Procedural Anxiety, Pain Catastrophizing.
What interventions are being tested in trial NCT05895383?
The interventions under investigation include: Nitrous oxide (DRUG).
Who is sponsoring clinical trial NCT05895383?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05895383 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Procedural 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 NCT05895383's enrollment target sits among peer trials
35 9th of 9 higher than 1 of 9 other Procedural Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Procedural 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.
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