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NCT02525718 · ClinicalTrials.gov registry record · Phase 2

Selective Intraoperative Administration of Local Anesthesia in Breast Reconstruction

A Phase 2 study, sponsored by Northwestern University.

Completed
Registry status
Phase 2
Development phase
47
Enrollment target

NCT02525718: Completed Phase 2 study, sponsored by Northwestern University.

NCT02525718 is a Phase 2 study that has completed, run by Northwestern University. The registered enrollment target is 47 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02525718, a Phase 2 study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
Phase 2
Development phase
47 participants
Enrollment target

Study Summary

Subjects are being asked to participate in this study because they will be undergoing unilateral (one) or bilateral (two) mastectomy surgery with immediate reconstruction involving insertion of a tissue expander.

Primary Outcome

The primary outcome measure is a well-validated and widely used survey measuring the quality of recovery from anesthesia entitled the "Global 40 Item Quality of Recovery" survey. This is a 40 question survey administered to patients to allow them to rate their quality of recovery along a number of different dimensions, including emotional state, physical comfort, psychological support, physical independence, and pain. The score ranges from 40 to 200, with 40 representing a very poor overall qual

Interventions

  • DRUG Saline
  • DRUG 0.25 % bupivacaine (2.5 mg/ml) w/ 1:100,000 epinephrine & 4 mg dexamethasone

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2015-08
Est. Completion 2017-03
Phase Phase 2
Northwestern University

1,209 total trials

What the finished NCT02525718 record still lists

NCT02525718 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% lower).

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

NCT02525718 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02525718 about?

NCT02525718 is a clinical study titled "Selective Intraoperative Administration of Local Anesthesia in Breast Reconstruction". Subjects are being asked to participate in this study because they will be undergoing unilateral (one) or bilateral (two) mastectomy surgery with immediate reconstruction involving insertion of a tissue expander.

What is the current status of trial NCT02525718?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 47 participants. The study started on 2015-08. Estimated completion is 2017-03.

What interventions are being tested in trial NCT02525718?

The interventions under investigation include: Saline (DRUG), 0.25 % bupivacaine (2.5 mg/ml) w/ 1:100,000 epinephrine & 4 mg dexamethasone (DRUG).

Who is sponsoring clinical trial NCT02525718?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02525718's enrollment target sits among peer trials

47 1283rd of 2000 higher than 715 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02525718, the US trial registry maintained by the National Library of Medicine. NCT02525718 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.