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NCT01122745 · ClinicalTrials.gov registry record

Single Shot vs Continuous Interscalene Block for Rotator Cuff Repair

A clinical trial of Pain and Surgery, sponsored by University of Chicago.

Completed
Registry status
88
Enrollment target
1
Study location

NCT01122745: Completed study of Pain and Surgery, sponsored by University of Chicago.

NCT01122745 is a study of Pain and Surgery that has completed, run by University of Chicago. The registered enrollment target is 88 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01122745, a study of Pain and Surgery, has completed, sponsored by University of Chicago.

COMPLETED
Registry status
88 participants
Enrollment target
1
Study location

Study Summary

1. Rotator cuff have painful post surgery recovery. 2. Single shot interscalene with oral analgesics may or may not be enough 3. Continuous nerve block may be too much for the surgery 4. The idea is to compare two techniques to see if the two techniques can improve patient pain control and satisfaction.

Primary Outcome

Patients having rotator cuff repair surgery will be randomized to either single shot or continuous catheter group. Pain score will be followed for 2 days to see which group gets better pain relief.

Study Locations (1)

Illinois

  • University of Chicago Hospitals - Chicago

Trial Details

FieldValue
Enrollment Target 88 participants
Start Date 2010-08
Est. Completion 2013-10
University of Chicago

796 total trials

What the finished NCT01122745 record still lists

NCT01122745 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 304-participant average among 374 other Pain trials with a reported enrollment target (71% lower).

The record links to 3 conditions, with Pain appearing as the primary indexed condition, and to 0 interventions.

NCT01122745 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT01122745 about?

NCT01122745 is a clinical study titled "Single Shot vs Continuous Interscalene Block for Rotator Cuff Repair". 1. Rotator cuff have painful post surgery recovery. 2. Single shot interscalene with oral analgesics may or may not be enough 3. Continuous nerve block may be too much for the surgery 4. The idea is to compare two techniques to see if the two techniques can improve patient pain control and satisfact...

What is the current status of trial NCT01122745?

This trial is currently completed. The enrollment target is 88 participants. The study started on 2010-08. Estimated completion is 2013-10.

What conditions does trial NCT01122745 study?

This clinical trial studies the following conditions: Pain, Surgery, Rotator Cuff.

Who is sponsoring clinical trial NCT01122745?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01122745 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01122745's enrollment target sits among peer trials

88 185th of 374 higher than 190 of 374 other Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pain 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 NCT01122745, the US trial registry maintained by the National Library of Medicine. NCT01122745 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.