Clinical Trials Directory

Trials / Completed

CompletedNCT02377687

Is Life Worth Living After Major Emergency GI Surgery? Patient Reported Outcome in Elderly Emergency Surgery Patients

Status
Completed
Phase
Study type
Observational
Enrollment
52 (actual)
Sponsor
Hvidovre University Hospital · Academic / Other
Sex
All
Age
75 Years
Healthy volunteers
Not accepted

Summary

To study the impact of emergency high risk GI surgery on HRQOL in elderly patients, seventy-five years or above and to explore the patients' experience with the informed consent process and the status 6 months after surgery.

Detailed description

We will identify all patients aged ≥ 75 having an emergency GI laparotomy or laparoscopy between the 1st of November 2014 and the 30st of April 2015. The first part of the study will take place in the first postoperative week, while the patient is in hospital. After consent we will ask both patient and relatives/caregivers questions concerning the preoperative course and the informed consent. We will ask for permission to call the patients for a followup (the second part of the study) 5-7 months after discharge and permission to contact their closest relative. The closest relative is chosen by the patient and will after consent be asked the same questions in the first postoperative week and after 6 months. The second part of the study will be initiated with a letter with SF-36 and an additional questionnaire . The SF-36 will be returned by letter. We will contact the patients by telephone 2 weeks after sending the letter ask them the questions from the additional questinaire. We will compare the results from the SF-36 with age-matched controls (Data from the Danish SF-36 Manual). If the patient is not capable of answering the questionnaires, the primary reason is noted (e.g. suffering from dementia or didn't speak Danish, dead). We will aim at a 6 month follow-up period after discharge allowing a range from 5-7 months. Data acquisition will be done in the fall 2014 until late 2015.

Conditions

Interventions

TypeNameDescription
OTHERobservational study

Timeline

Start date
2014-11-01
Primary completion
2015-11-01
Completion
2015-11-01
First posted
2015-03-03
Last updated
2016-02-24

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT02377687. Inclusion in this directory is not an endorsement.