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NCT02068677 · ClinicalTrials.gov registry record · NA

Evaluation of Injection Techniques in Celiac Plexus Neurolysis

A NA study, sponsored by AdventHealth.

Completed
Registry status
NA
Development phase
51
Enrollment target

NCT02068677: Completed NA study, sponsored by AdventHealth.

NCT02068677 is a NA study that has completed, run by AdventHealth. The registered enrollment target is 51 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02068677, a NA study, has completed, sponsored by AdventHealth.

COMPLETED
Registry status
NA
Development phase
51 participants
Enrollment target

Study Summary

1\. To evaluate the efficacy of EUS-CPN in subjects who experience a sympathetic response during injection when compared with subjects who do not experience sympathetic response during injection. EUS-CPN when performed in subjects who experience a sympathetic response during injection will have better pain relief when compared to subjects who do not experience a sympathetic response during injection.

Primary Outcome

The primary endpoint of the study is abdominal pain. It will be assessed with a standardized 11-point continuous visual analog pain scale with "0" equaling no pain, "5" moderate pain and "10" worst pain ever. Before the procedure, patient will be instructed in the use of the pain scale by the research nurse. After the procedure, pain scores will be assessed by the clinical research nurse at the predetermined intervals. A complete response will be defined as an absence of abdominal pain requirin

Interventions

  • OTHER Sympathetic response
  • OTHER no sympathetic response

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2013-08
Est. Completion 2014-11
Phase NA
AdventHealth

95 total trials

What the finished NCT02068677 record still lists

NCT02068677 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Sympathetic response is the first listed.

NCT02068677 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02068677 about?

NCT02068677 is a clinical study titled "Evaluation of Injection Techniques in Celiac Plexus Neurolysis". 1\. To evaluate the efficacy of EUS-CPN in subjects who experience a sympathetic response during injection when compared with subjects who do not experience sympathetic response during injection. EUS-CPN when performed in subjects who experience a sympathetic response during injection will have bet...

What is the current status of trial NCT02068677?

This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2013-08. Estimated completion is 2014-11.

What interventions are being tested in trial NCT02068677?

The interventions under investigation include: Sympathetic response (OTHER), no sympathetic response (OTHER).

Who is sponsoring clinical trial NCT02068677?

This trial is sponsored by AdventHealth, which has 95 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02068677's enrollment target sits among peer trials

51 1279th of 2000 higher than 722 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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Source: ClinicalTrials.gov NCT02068677, the US trial registry maintained by the National Library of Medicine. NCT02068677 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.