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Feasibility of Ambulatory Surgery for Early Breast Cancer

NCT01613352 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2012-06-07

No results posted yet for this study

Summary

The aim was to assess the patient compliance and medical and psychosocial effects of same day hospital discharge after breast conserving surgery and sentinel node biopsy only.

Conditions

  • Early Breast Cancer
  • Psychosocial Wellbeing
  • Ambulatory Surgery

Interventions

OTHER

Ambulatory surgery

Sentinel node mapping was done on the previous day and the patients were operated on first in the morning.

Sponsors & Collaborators

  • Helsinki University Central Hospital

    lead OTHER

Principal Investigators

  • Jaana H Vironen, MD, PhD · Helsinki University Central Hospital, Jorvi Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2011-04-30
Completion
2011-04-30

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01613352 on ClinicalTrials.gov