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NCT02670057 · ClinicalTrials.gov registry record · NA
Sphenopalatine Ganglion Block to Treat Shoulder Pain During and/or After Cesarean
A NA study, sponsored by NYU Langone Health.
- Completed
- Registry status
- NA
- Development phase
- 117
- Enrollment target
NCT02670057: Completed NA study, sponsored by NYU Langone Health.
NCT02670057 is a NA study that has completed, run by NYU Langone Health. The registered enrollment target is 117 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02670057, a NA study, has completed, sponsored by NYU Langone Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 117 participants
- Enrollment target
Study Summary
The purpose of this open label pilot study is to evaluate the utility of sphenopalatine ganglion (SPG) block to manage ipsilateral shoulder pain (ISP) during and/or after cesarean.
Interventions
- PROCEDURE Transnasal SPG block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 117 participants |
| Start Date | 2015-11 |
| Est. Completion | 2017-12-12 |
| Phase | NA |
What the finished NCT02670057 record still lists
NCT02670057 is an interventional study that assigns participants to a tested intervention. The registered 117 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 1 intervention - of which Transnasal SPG block is the first listed.
NCT02670057 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02670057 about?
NCT02670057 is a clinical study titled "Sphenopalatine Ganglion Block to Treat Shoulder Pain During and/or After Cesarean". The purpose of this open label pilot study is to evaluate the utility of sphenopalatine ganglion (SPG) block to manage ipsilateral shoulder pain (ISP) during and/or after cesarean.
What is the current status of trial NCT02670057?
This trial is currently completed. It is a NA study. The enrollment target is 117 participants. The study started on 2015-11. Estimated completion is 2017-12-12.
What interventions are being tested in trial NCT02670057?
The interventions under investigation include: Transnasal SPG block (PROCEDURE).
Who is sponsoring clinical trial NCT02670057?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02670057's enrollment target sits among peer trials
117 807th of 2000 higher than 1,193 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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