← Back to Search

Experimental for Breast Reconstruction (RESTORE Trial)

N/A
Waitlist Available
Led By Sophocles Voineskos, MD, MSc.
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Women 18 years of age or older
Able to understand and communicate in English
Timeline
Screening 3 weeks
Treatment Varies
Follow Up this will be calculated through study completion, an average of 1 year, at the time when every enrolled participant is set to complete the final follow up.
Awards & highlights

RESTORE Trial Summary

Educational Session To Optimize Patient's Breast Reconstruction Experience at McMaster

Eligible Conditions
  • Breast Reconstruction
  • Patient Education

RESTORE Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

RESTORE Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~this will be calculated through study completion, an average of 1 year, at the time when every enrolled participant is set to complete the final follow up.
This trial's timeline: 3 weeks for screening, Varies for treatment, and this will be calculated through study completion, an average of 1 year, at the time when every enrolled participant is set to complete the final follow up. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Feasibility of the research study as measured by retention rate
Secondary outcome measures
Anxiety
Feasibility measure: Budget assessment
Feasibility measure: Compliance rate
+7 more

RESTORE Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
The experimental group will receive an additional educational session before their operation about what to expect during their reconstructive journey, in addition to the current standard educational information from the surgeon along with an information package.
Group II: ControlActive Control1 Intervention
The control group will receive the current standard educational information from the surgeon along with an information package.

Find a Location

Who is running the clinical trial?

McMaster UniversityLead Sponsor
879 Previous Clinical Trials
2,596,926 Total Patients Enrolled
1 Trials studying Breast Reconstruction
722 Patients Enrolled for Breast Reconstruction
Sophocles Voineskos, MD, MSc.Principal InvestigatorMcMaster University

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~9 spots leftby Mar 2025