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NCT01701115 · ClinicalTrials.gov registry record · NA
Effect of Local Anesthetic Dose on Interscalene Block
A NA study, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 154
- Enrollment target
NCT01701115: Completed NA study, sponsored by Hospital for Special Surgery, New York.
NCT01701115 is a NA study that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 154 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01701115, a NA study, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 154 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if a decrease in the standard volume of local anesthetic used to numb your shoulder area before shoulder arthroscopy will provide adequate anesthesia for the procedure and decrease the amount of time until you are ready for discharge from the hospital.
Primary Outcome
The primary outcome will be handgrip strength as measured by a dynamometer. A reading will be obtained at baseline (before the interscalene block) and 60 minutes post-operative.
Interventions
- PROCEDURE Low Dose (20 ml) Local Anesthetic Volume for Interscalene Block
- PROCEDURE Control Dose (40 mL) Local Anesthetic Volume for Interscalene Block
- DRUG Low Dose (20 mL) Local Anesthetic (Mepivacaine:Bupivacaine)
- DRUG Control Dose (40 mL) Local Anesthetic (Mepivacaine:Bupivacaine)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 154 participants |
| Start Date | 2012-08 |
| Est. Completion | 2013-08 |
| Phase | NA |
What the finished NCT01701115 record still lists
NCT01701115 is an interventional study that assigns participants to a tested intervention. The registered 154 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 (89% lower).
The record links to 0 conditions, and to 4 interventions - of which Low Dose (20 ml) Local Anesthetic Volume for Interscalene Block is the first listed.
NCT01701115 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01701115 about?
NCT01701115 is a clinical study titled "Effect of Local Anesthetic Dose on Interscalene Block". The purpose of this study is to determine if a decrease in the standard volume of local anesthetic used to numb your shoulder area before shoulder arthroscopy will provide adequate anesthesia for the procedure and decrease the amount of time until you are ready for discharge from the hospital.
What is the current status of trial NCT01701115?
This trial is currently completed. It is a NA study. The enrollment target is 154 participants. The study started on 2012-08. Estimated completion is 2013-08.
What interventions are being tested in trial NCT01701115?
The interventions under investigation include: Low Dose (20 ml) Local Anesthetic Volume for Interscalene Block (PROCEDURE), Control Dose (40 mL) Local Anesthetic Volume for Interscalene Block (PROCEDURE), Low Dose (20 mL) Local Anesthetic (Mepivacaine:Bupivacaine) (DRUG), Control Dose (40 mL) Local Anesthetic (Mepivacaine:Bupivacaine) (DRUG).
Who is sponsoring clinical trial NCT01701115?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01701115's enrollment target sits among peer trials
154 656th of 2000 higher than 1,345 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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