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NCT01415193 · ClinicalTrials.gov registry record · NA
Tibial Nerve Versus Sciatic Nerve Block
A NA study of Post Operative Analgesia, sponsored by Trinity Health Of New England.
- Completed
- Registry status
- NA
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT01415193: Completed NA study of Post Operative Analgesia, sponsored by Trinity Health Of New England.
NCT01415193 is a NA study of Post Operative Analgesia that has completed, run by Trinity Health Of New England. The registered enrollment target is 80 participants, below the 114-participant average among 5 other Post Operative Analgesia trials with a reported enrollment target (30% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01415193, a NA study of Post Operative Analgesia, has completed, sponsored by Trinity Health Of New England.
- COMPLETED
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to analyse the ability to selectively block the posterior tibial nerve sparing the function of the common peritoneal nerve. To assess the efficacy of blocking the posterior tibial nerve will give the same post-operative pain relief after total knee surgery compared to a sciatic nerve block.
Primary Outcome
Measure frequency of foot drop in two groups and compare results.
Conditions Studied
Interventions
- PROCEDURE Selective Tibial Nerve block
- PROCEDURE Sciatic Nerve Block
Study Locations (1)
Connecticut
- Saint Francis Hospital and Medical Center - Hartford
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2009-03 |
| Est. Completion | 2010-12 |
| Phase | NA |
What the finished NCT01415193 record still lists
NCT01415193 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 114-participant average among 5 other Post Operative Analgesia trials with a reported enrollment target (30% lower).
The record links to 1 condition, with Post Operative Analgesia appearing as the primary indexed condition, and to 2 interventions - of which Selective Tibial Nerve block is the first listed.
NCT01415193 reports a single indexed study location in Connecticut.
Frequently Asked Questions
What is clinical trial NCT01415193 about?
NCT01415193 is a clinical study titled "Tibial Nerve Versus Sciatic Nerve Block". The purpose of this study is to analyse the ability to selectively block the posterior tibial nerve sparing the function of the common peritoneal nerve. To assess the efficacy of blocking the posterior tibial nerve will give the same post-operative pain relief after total knee surgery compared to a ...
What is the current status of trial NCT01415193?
This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2009-03. Estimated completion is 2010-12.
What conditions does trial NCT01415193 study?
This clinical trial studies the following conditions: Post Operative Analgesia.
What interventions are being tested in trial NCT01415193?
The interventions under investigation include: Selective Tibial Nerve block (PROCEDURE), Sciatic Nerve Block (PROCEDURE).
Who is sponsoring clinical trial NCT01415193?
This trial is sponsored by Trinity Health Of New England, which has 20 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01415193 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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