Development of a Patient-Reported Outcome Measures to Detect Perioperative Symptom Burden Following Major Abdominal Surgery for Cancer

Recruiting

• Conditions: C15; C16; C17; C18; C19; C20; C21; C22; C23; C24

• Registration Number: DRKS00023193
• Lead Sponsor: niversitätsklinikum Mannheim

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-03-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 350

Inclusion Criteria

1. Age = 18 years
2. major abdominal surgery for gastrointestinal malignancies
defined as:
3. Minimally-invasive or open surgery
4. Written informed consent
5. Ability and willingness to respond to questionnaires

Exclusion Criteria

1. ASA > 4
2. Impaired mental state or language problems

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Development of a Patient-Reported Outccome Measure

Secondary Outcome Measures

Name	Time	Method
Symptom burden, Intraoperative Outcomes,<br>Postoperative Complications, Use of healthcare resources, Time-to-functional recovery, Quality of life (Patient and Caregiver)