- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05442164
Effect of Implementation of the Danish Emergency Surgery (DANAKIR) Support Network on Post-discharge Outcomes After Major Emergency Abdominal Surgery (DANAKIR)
Effect of Implementation of the Danish Emergency Surgery (DANAKIR) Support Network on Post-discharge Outcomes After Major Emergency Abdominal Surgery: a Prospective Before And-after Study
Effect of implementation of the Danish Emergency Surgery (DANAKIR) support Network on post-discharge outcomes after major emergency abdominal surgery: a prospective before and-after study
Background Major emergency abdominal surgery is performed in more than 5000 patients yearly in Denmark. In general, little is known about the period after the discharge of these patients besides that chronic pain, physical dysfunction, and quality of life are severely affected in up to 50% of patients at long-term follow-up. A recent study investigating unplanned readmission after major emergency abdominal surgery found that up to 50% undergo unplanned readmission within the first 180 days after discharge.
Purpose The purpose of this study is to evaluate the effects of inviting patients undergoing major emergency surgery and their relatives to join a support network after discharge (the DANAKIR network).
Methods This study is designed as a before- and after study. Prior to establishing the DANAKIR (Danish Emergency Surgery Network) support network, the investigators will consecutively during a one year inclusion period prospectively include all patients undergoing emergency abdominal surgery with a midline laparotomy. The inclusion period starts 1st August 2021.
The investigators will register the following in the pre-implementation phase:
- Postoperative day (POD) 30: Quality of life (EQ-5D-5L) (by telephone)
- POD90: Quality of life (EQ-5D-5L) (by telephone), readmissions (by hospital file)
- POD 180: Quality of life (EQ-5D-5L) (by telephone), readmissions (by hospital file)
- Number of days at home with 90 days (by hospital file)
- Number of participants with at least one readmission (by hospital file) Hereafter the investigators will establish the DANAKIR support network. The investigators plan for a six-month inclusion period with DANAKIR starting 1th of September 2022
Intervention
The DANAKIR intervention will consist of:
- Structured written discharge information for the participanats and relatives about expectations and precautions
- Invitation to the DANAKIR monthly information meeting All patients undergoing emergency abdominal surgery and members of their family are invited to participate in at least one DANAKIR meeting. Patients and their relatives can participate in as many meetings as they wish; however, we encourage all patients to participate at least once.
DANAKIR meetings The monthly meetings are a core component of the support network. One time each month, a meeting will be held at Herlev Hospital with the participation of an emergency surgeon, an emergency surgery dedicated nurse, a dietician, and a physiotherapist. Furthermore, there will be research personnel present. Each professional (surgeon, nurse, dietician, physiotherapist) will host an informative 15 minute session regarding the postoperative course after major emergency surgery. Following the presentations time for questions in plenum and private with the different experts will be held. Furthermore, there will be an opportunity for networking at the DANAKIR meeting. Each meeting is planned to last 2 hours. At the end of each meeting the patients will be asked to evaluate the meeting and content.
Outcome measures The primary outcome of this study is the number of days at home within 90 days of surgery. The secondary outcomes are quality of life at 30 days, 90 days, and 180 days after surgery and the number of patients with at least one emergency readmission 90 days and 180 days from surgery.
Trial size The investigators expect to include 200 patients in the before group and 200 patients in the after group.
Perspectives The DANAKIR support network examines if a structure with physical network meetings is effective in regard to quality of life and preventing readmissions after major emergency surgery. The investigators hypothesize that the days at home will increase within 90 days from surgery and that quality of life will increase for both participants and their relatives by implementing a simple and obvious solution. If the DANAKIR network proves efficient it is an easily implemented solution to increase quality of life and days at home after major emergency surgery.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Dunja K Gellert-Kristensen, MD, PhD
- Phone Number: 28776364
- Email: dunja.kokotovic.gellert-kristensen@regionh.dk
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Emergency open, laparoscopic or laparoscopically assisted procedures involving: stomach, small bowel, large bowel, or rectum for conditions such as perforation, ischemia, abdominal abscess, bleeding, haematoma, or obstruction
- Bowel resection due to incarcerated incisional, umbilical, inguinal, and femoral hernias (but not hernia repair without bowel resection/repair)
- Laparoscopic/open adhesiolysis
- Fascial dehiscence
- Emergency surgery after elective surgery if criteria above is met
Exclusion Criteria:
- Elective procedures
- Appendectomy +/- drainage of localized abscess
- Cholecystectomy +/- drainage of localized abscess
- Emergency hernia repair without bowel resection
- Large-bowel endoscopic stent procedures
- Superficial wound dehiscence above the fascia
- Ruptured ectopic pregnancy or pelvic abscess due to inflammatory disease
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Before-group
Patients undergoing major emergency surgery before a supportive network is established
|
|
|
After-group
Patients undergoing major emergency surgery after a supportive network is established
|
The DANAKIR intervention will consist of:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Days at home within 90 days
Time Frame: 90 day
|
Number of days at home within 90 days of surgery
|
90 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life
Time Frame: Day 30, day 90, day 180
|
EQ-5D-5L
|
Day 30, day 90, day 180
|
|
Readmission
Time Frame: Day 90 and day 180
|
number of patients with at least one emergency readmission
|
Day 90 and day 180
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DANAKIR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Bowel Obstruction
-
The First Affiliated Hospital with Nanjing Medical...CompletedSmall Bowel Obstruction | Small Bowel Obstruction AdhesionChina
-
Florida Hospital Tampa Bay DivisionCompletedColectomy | Small Bowel Obstruction | Bowel Surgeries
-
North-Western State Medical University named after...RecruitingSmall Bowel Obstruction | Small Bowel Obstruction Adhesion | Small-Bowel Obstruction Due to Volvulus | Hernia IncarceratedRussian Federation
-
Roswell Park Cancer InstituteTerminatedMalignant Bowel ObstructionUnited States
-
Yale UniversityTerminatedSmall Bowel ObstructionUnited States
-
University of California, Los AngelesNot yet recruiting
-
Danish Small Bowel Obstruction CollaborativeActive, not recruiting
-
Helsinki University Central HospitalCompleted
-
University of TartuNorth Estonian Medical CenterCompleted
-
Groupe Hospitalier Paris Saint JosephActive, not recruiting
Clinical Trials on DANAKIR support network
-
University of ChicagoUniversity of Alabama at Birmingham; Tulane University; Birmingham AIDS Outreach and other collaboratorsRecruitingHIV SeropositivityUnited States
-
Hennepin Healthcare Research InstituteUniversity of MinnesotaCompletedKidney TransplantUnited States
-
Hennepin Healthcare Research InstituteUniversity of MinnesotaRecruitingKidney TransplantUnited States
-
Medical College of WisconsinNational Institute of Mental Health (NIMH)CompletedHIV | AIDSUnited States, Russian Federation
-
University of the PhilippinesPhilippine Dermatological SocietyCompleted
-
Royal Marsden NHS Foundation TrustImperial College London; Institute of Cancer Research, United KingdomActive, not recruiting
-
University of California, DavisCompletedBehavior, HealthUnited States
-
University of British ColumbiaBrainTrust Canada; ABI Wellness; The Kelowna Women's Shelter; Nanaimo Brain Injury...RecruitingMild Traumatic Brain InjuryCanada
-
Wake Forest University Health SciencesNational Institute of Mental Health (NIMH)CompletedHIV/AIDSUnited States, South Africa
-
UConn HealthNational Institute on Alcohol Abuse and Alcoholism (NIAAA)Completed