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NCT01355757 · ClinicalTrials.gov registry record · Early Phase 1

Post-Operative Quality of Life Evaluation for Different Anesthesia Techniques for Arthroscopic Shoulder Surgery

A Early Phase 1 study, sponsored by St. Luke's-Roosevelt Hospital Center.

Completed
Registry status
Early Phase 1
Development phase
70
Enrollment target

NCT01355757: Completed Early Phase 1 study, sponsored by St. Luke's-Roosevelt Hospital Center.

NCT01355757 is a Early Phase 1 study that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 70 participants, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (32% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01355757, a Early Phase 1 study, has completed, sponsored by St. Luke's-Roosevelt Hospital Center.

COMPLETED
Registry status
Early Phase 1
Development phase
70 participants
Enrollment target

Study Summary

Randomized controlled trial on efficacy of single injection or continuous interscalene brachial plexus block on analgesia in patients having outpatient rotator cuff surgery.

Primary Outcome

To describe rehabilitation achievement and quality of life during 24-week follow-up after shoulder arthroscopy and rotator cuff repair, and identify any association between type of anesthesia procedure and patients' quality of life

Interventions

  • DEVICE Baxter INFUSOR System
  • DRUG Single Injection of Local Anesthetic

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2011-06
Est. Completion 2013-01
Phase Early Phase 1

What the finished NCT01355757 record still lists

NCT01355757 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (32% higher).

The record links to 0 conditions, and to 2 interventions - of which Baxter INFUSOR System is the first listed.

NCT01355757 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01355757 about?

NCT01355757 is a clinical study titled "Post-Operative Quality of Life Evaluation for Different Anesthesia Techniques for Arthroscopic Shoulder Surgery". Randomized controlled trial on efficacy of single injection or continuous interscalene brachial plexus block on analgesia in patients having outpatient rotator cuff surgery.

What is the current status of trial NCT01355757?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 70 participants. The study started on 2011-06. Estimated completion is 2013-01.

What interventions are being tested in trial NCT01355757?

The interventions under investigation include: Baxter INFUSOR System (DEVICE), Single Injection of Local Anesthetic (DRUG).

Who is sponsoring clinical trial NCT01355757?

This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01355757's enrollment target sits among peer trials

70 339th of 2000 higher than 1,646 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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 NCT01355757, the US trial registry maintained by the National Library of Medicine. NCT01355757 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.