Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01385449 · ClinicalTrials.gov registry record · NA

Prospective Evaluation of Interscalene Nerve Catheters vs. Single Injection Blocks

A NA study, sponsored by University of Wisconsin, Madison.

Terminated
Registry status
NA
Development phase
73
Enrollment target

NCT01385449: Clinical Trial NA study, sponsored by University of Wisconsin, Madison.

NCT01385449 is a NA study that was terminated before completion, run by University of Wisconsin, Madison. The registered enrollment target is 73 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01385449, a NA study, was terminated before completion, sponsored by University of Wisconsin, Madison.

TERMINATED
Registry status
NA
Development phase
73 participants
Enrollment target

Study Summary

The primary hypothesis is that those patients who choose an interscalene catheter will have less pain postoperatively than those with single injection blocks. Secondary hypotheses examine physical therapy outcomes and incidence of parasthesia or pain following surgery for up to 3 months.

Primary Outcome

Pain score on post-operative day 1(POD1) using numeric rating scale (NRS)

Interventions

  • PROCEDURE interscalene catheter
  • PROCEDURE interscalene block

Trial Details

FieldValue
Enrollment Target 73 participants
Start Date 2011-06
Est. Completion 2016-02
Phase NA
University of Wisconsin, Madison

1,039 total trials

Why NCT01385449 stopped before completion

NCT01385449 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 73 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

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

NCT01385449 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01385449 about?

NCT01385449 is a clinical study titled "Prospective Evaluation of Interscalene Nerve Catheters vs. Single Injection Blocks". The primary hypothesis is that those patients who choose an interscalene catheter will have less pain postoperatively than those with single injection blocks. Secondary hypotheses examine physical therapy outcomes and incidence of parasthesia or pain following surgery for up to 3 months.

What is the current status of trial NCT01385449?

This trial is currently terminated. It is a NA study. The enrollment target is 73 participants. The study started on 2011-06. Estimated completion is 2016-02.

What interventions are being tested in trial NCT01385449?

The interventions under investigation include: interscalene catheter (PROCEDURE), interscalene block (PROCEDURE).

Who is sponsoring clinical trial NCT01385449?

This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01385449's enrollment target sits among peer trials

73 1089th of 2000 higher than 912 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03661307 · 73 participants · Phase 1

    Quizartinib, Decitabine, and Venetoclax in Treating Participants With Untreated or Relapsed Acute Myeloid Leukemia or High Risk Myelodysplastic Syndrome

  • NCT05386108 · 73 participants · Phase 1

    Study of Abemaciclib and Elacestrant in Participants With Brain Metastasis Due to ER+/HER-2- Breast Cancer

  • NCT05961592 · 73 participants · Phase 1

    R-2487 in Patients With Rheumatoid Arthritis

  • NCT06150664 · 73 participants · Phase 1

    A Phase 1 of CTX-8371 in Patients With Advanced Malignancies

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01385449, the US trial registry maintained by the National Library of Medicine. NCT01385449 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.