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Electronic Reporting of Symptoms After Surgery

NCT02700256 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 135

Last updated 2019-11-04

No results posted yet for this study

Summary

The purpose of this pilot study is to find out if patients are willing to self-report symptoms in the first 5 days following discharge, or when they leave the hospital after "ambulatory surgery" ("ambulatory surgery" is when the patient has surgery and then goes home within 24 hours).

Conditions

  • Patients Scheduled to Undergo Surgery on the Gynecology Service

Interventions

BEHAVIORAL

survey

All patients will submit a baseline survey following enrollment onto study. After successful completion of the AXR or 24-hour discharge pathway, the consented patient will be contacted by email or telephone for 5 days following discharge from surgery.

Sponsors & Collaborators

Principal Investigators

  • Oliver Zivanovic, MD, PhD · Memorial Sloan Kettering Cancer Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-04
Primary Completion
2019-10-21
Completion
2019-10-21

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02700256 on ClinicalTrials.gov