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Quality of Life in Acute Complicated and Chronic Recurrent Left-sided Diverticulitis (DATE)

Primary Purpose

Diverticulitis of Sigmoid

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Sigmoid resection
Sponsored by
Kepler University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diverticulitis of Sigmoid focused on measuring Recurrent diverticulitis, Quality of life, Acute complicated Diverticulitis, Early resection, Elective resection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Informed consent to participate in the study CDD Type 2a, 2b: acute complicated left-sided diverticulitis CDD Type 3b: relapsing diverticulitis without complications (>2 episodes within 2 years) Acute presentation Inflammation located in the left-sided colon Inflammation is CT proven or ultrasound confirmed from experienced radiologists Exclusion Criteria: < 18 years Pregnancy BMI > 55kg/m2 Current colorectal carcinoma in the left-sided colon Oral and/or intravenous corticosteroid Ongoing chemotherapy Status post left hemicolectomy Patients who cannot take care of themselves at home or are unable to follow instructions Patients who are not fit for surgery (anesthesia, expert knowledge from specialists) and will not benefit from surgery

Sites / Locations

  • Krankenhaus Barmherzige Schwestern LinzRecruiting
  • Kepler University HospitalRecruiting
  • Ordensklinikum Elisabethinen LinzRecruiting
  • Universitätsklinikum Mannheim

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Group A (Early)

Group B (Late)

Arm Description

Early left hemicolectomy immediately up to a maximum of 2 days after 7-10 days lasting initial conservative or interventional treatment (e.g: antibiotics, analgesics, drainage) and CT scan/ultrasound proven left-sided colonic diverticulitis

Elective left hemicolectomy 6 to 8 weeks after 7-10 days lasting initial conservative or interventional treatment (e.g: antibiotics, analgesics, drainage) and CT scan/ultrasound proven left-sided colonic diverticulitis

Outcomes

Primary Outcome Measures

Gastrointestinal Quality of Life Index
Quality of Life

Secondary Outcome Measures

SF-36 score (Short form score)
physical and mental health summary scores (0-100), the higher the better
Low anterior resection syndrome score
points (0-40), the lower the better
Anastomosis insufficiency
yes/no
Intraoperative complication
bleeding, ureter harming (yes/no)
Exitus
yes/no
Length of stay (sum of days in hospital until end of study)
days
Earlier readmission due to recurrence while waiting for surgery
Only in Group B
Postoperative complication
pneumonia, urinary tract infection (yes/no)

Full Information

First Posted
June 7, 2023
Last Updated
July 19, 2023
Sponsor
Kepler University Hospital
Collaborators
Krankenhaus Barmherzige Schwestern Linz, Elisabethinen Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05942833
Brief Title
Quality of Life in Acute Complicated and Chronic Recurrent Left-sided Diverticulitis
Acronym
DATE
Official Title
DATE Trial: Outcomes and Quality of Life in Patients With Early Versus Elective Resection in Acute Complicated and Chronic Recurrent Left-sided Diverticulitis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 16, 2023 (Actual)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kepler University Hospital
Collaborators
Krankenhaus Barmherzige Schwestern Linz, Elisabethinen Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Patients presenting in hospital with symptoms of acute diverticulitis. Acute inflammation of the left-sided colon is confirmed with CT scan or ultrasound in experienced centers and diagnosis is defined according to the "Classification of Diverticular Disease (CDD)". CDD Type 2a, 2b and 3b will be included and then randomized in two groups. Group A will get an early left hemicolectomy 7 to 10 days after admission and initial antibiotic therapy and/or drainage of the abscess. Group B is designated for an elective resection 6 to 8 weeks after dismissal at the earliest and initial conservative treatment and/or after drainage of the abscess. Six weeks after the operation patients of Group A will be asked for their present quality of life with a standardized scoring system (Gastrointestinal Quality of Life Index = GIQLI; Short-form 36 Score = SF-36 Score; Low anterior resection syndrome = LARS Score). Group B (elective resection) will be asked at their readmission prior to elective surgery is done. This survey package will be repeated again 6 to 8 weeks later in both groups. Primary endpoints will be the two GIQLI at the said examination times. Secondary endpoints will be SF-36 score, LARS-score, GIQLI-Domains, anastomosis insufficiency and other complications, mortality and length of hospital stay. Comparisons between the groups are made at the said examination times but also 6-8 weeks after the operation.
Detailed Description
Primary endpoints: Gastrointestinal Quality of Life Index (GIQLI) Secondary endpoints: SF-36 score (physical and mental health summary scores), LARS score, GIQLI-domains, anastomosis insufficiency and other complications, exitus and length of hospital stay Treatment strategy: A patient is coming into the hospital with acute symptoms of diverticulitis. The diagnosis must then be confirmed either with ultrasound or with a CT scan. After confirmation the patient is asked to be part of the study. At that point of time the patient does not know his randomization. After the patient's approval and signed consent the patients will bei informed about the further procedure and the appointment of surgery. Questionnaires will now be filled out and antibiotical treatment starts. If necessary a radiological intervention (drainage) is performed. Is the patient is randomized into Group A he will get early left hemicolectomy immediately up to a maximum of 2 days after 7-10 days lasting initial conservative or interventional treatment (e.g: antibiotics, analgesics, drainage). If the patient is in Group B he will receive an elective left hemicolectomy 6 to 8 weeks after 7-10 days lasting initial conservative or interventional treatment (e.g: antibiotics, analgesics, drainage). Reassessment of the questionnaires will bei done in both groups. Group A will be asked 6-8 after surgery and again 6-8 weeks after the second reassessment. Group B will be asked 6-8 weeks after discharge (directly before surgery) and again 6-8 weeks after surgery. The aim of the study is to evaluate the outcome and quality of life in patients receiving early surgery versus elective resection of the left-sided colon in acute complicated diverticulitis and chronic recurrent diverticulitis with acute exacerbation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diverticulitis of Sigmoid
Keywords
Recurrent diverticulitis, Quality of life, Acute complicated Diverticulitis, Early resection, Elective resection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective, randomized controlled
Masking
None (Open Label)
Allocation
Randomized
Enrollment
136 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A (Early)
Arm Type
Experimental
Arm Description
Early left hemicolectomy immediately up to a maximum of 2 days after 7-10 days lasting initial conservative or interventional treatment (e.g: antibiotics, analgesics, drainage) and CT scan/ultrasound proven left-sided colonic diverticulitis
Arm Title
Group B (Late)
Arm Type
Other
Arm Description
Elective left hemicolectomy 6 to 8 weeks after 7-10 days lasting initial conservative or interventional treatment (e.g: antibiotics, analgesics, drainage) and CT scan/ultrasound proven left-sided colonic diverticulitis
Intervention Type
Procedure
Intervention Name(s)
Sigmoid resection
Intervention Description
Timing of sigmoid resection
Primary Outcome Measure Information:
Title
Gastrointestinal Quality of Life Index
Description
Quality of Life
Time Frame
Up to 18 weeks
Secondary Outcome Measure Information:
Title
SF-36 score (Short form score)
Description
physical and mental health summary scores (0-100), the higher the better
Time Frame
Up to 18 weeks
Title
Low anterior resection syndrome score
Description
points (0-40), the lower the better
Time Frame
Up to 18 weeks
Title
Anastomosis insufficiency
Description
yes/no
Time Frame
Up to 18 weeks
Title
Intraoperative complication
Description
bleeding, ureter harming (yes/no)
Time Frame
Up to 18 weeks
Title
Exitus
Description
yes/no
Time Frame
Up to 18 weeks
Title
Length of stay (sum of days in hospital until end of study)
Description
days
Time Frame
Up to 18 weeks
Title
Earlier readmission due to recurrence while waiting for surgery
Description
Only in Group B
Time Frame
Up to 18 weeks
Title
Postoperative complication
Description
pneumonia, urinary tract infection (yes/no)
Time Frame
Up to 18 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent to participate in the study CDD Type 2a, 2b: acute complicated left-sided diverticulitis CDD Type 3b: relapsing diverticulitis without complications (>2 episodes within 2 years) Acute presentation Inflammation located in the left-sided colon Inflammation is CT proven or ultrasound confirmed from experienced radiologists Exclusion Criteria: < 18 years Pregnancy BMI > 55kg/m2 Current colorectal carcinoma in the left-sided colon Oral and/or intravenous corticosteroid Ongoing chemotherapy Status post left hemicolectomy Patients who cannot take care of themselves at home or are unable to follow instructions Patients who are not fit for surgery (anesthesia, expert knowledge from specialists) and will not benefit from surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sandra Raab, Dr.
Phone
+43 (0)5 7680 83 - 78470
Email
sandra.raab@kepleruniklinikum.at
First Name & Middle Initial & Last Name or Official Title & Degree
Andreas Shamiyeh, Dr.
Phone
+43 (0)5 7680 83 - 2133
Email
andreas.shamiyeh@kepleruniklinikum.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas Shamiyeh, Dr.
Organizational Affiliation
Kepler University Hospital Linz
Official's Role
Principal Investigator
Facility Information:
Facility Name
Krankenhaus Barmherzige Schwestern Linz
City
Linz
State/Province
Upper Austria
ZIP/Postal Code
4010
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthias Biebl, Dr.
Phone
+43 (0)732-7677 - 7300
Email
matthias.biebl@ordensklinikum.at
First Name & Middle Initial & Last Name & Degree
Gerd Pressl, Dr.
Phone
+43 732 7677 - 7300
Email
gerd.pressl@ordensklinikum.at
Facility Name
Kepler University Hospital
City
Linz
State/Province
Upper Austria
ZIP/Postal Code
4020
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra Raab, Dr.
Phone
+43 (0)5 7680 83 - 78470
Email
sandra.raab@kepleruniklinikum.at
First Name & Middle Initial & Last Name & Degree
Andreas Shamiyeh, Dr.
Phone
+43 (0)5 7680 83 - 2133
Email
andreas.shamiyeh@kepleruniklinikum.at
Facility Name
Ordensklinikum Elisabethinen Linz
City
Linz
ZIP/Postal Code
4020
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthias Biebl, Dr.
Phone
+43 (0)732-7677 - 7300
Email
matthias.biebl@ordensklinikum.at
First Name & Middle Initial & Last Name & Degree
Christoph Schwaiger-Hengstschläger, Dr.
Phone
+43 (0)732-7677 - 7300
Facility Name
Universitätsklinikum Mannheim
City
Mannheim
ZIP/Postal Code
68167
Country
Germany
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Steffen Seyfried, PD MD
Phone
+49 621 383-4864
Email
steffen.seyfried@umm.de
First Name & Middle Initial & Last Name & Degree
Christoph Reißfelder, Prof. MD
Phone
+49 621 383-4864
Email
christoph.reißfelder@umm.de

12. IPD Sharing Statement

Learn more about this trial

Quality of Life in Acute Complicated and Chronic Recurrent Left-sided Diverticulitis

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