Italian Study Group on Complicated Diverticulosis
GISDIC
1 other identifier
observational
N/A
1 country
1
Brief Summary
Patients were recruited over a four year period from 1996 to 1999. Those admitted in the years 1996 and 1997 were retrospectively accrued from the clinical records, while patients treated between 1998 and 1999 patients were entered on the database prospectively on admission. Inclusion criteria All consecutive patients with left sided acute diverticulitis diagnosed clinically by the presence of abdominal pain, associated with leukocytosis (\>11x109) and/or fever \>38°C, confirmed by imaging (CT scan, ultrasonography, water soluble contrast enema) either alone or in combination and/or by operative findings, entered the study. The CT criteria for the diagnosis included a localized thickening (≥4 mm) of the colonic wall and signs of inflammation of the pericolic fat, with abscess and/or extraluminal air and/or extraluminal contrast. The criteria for ultrasound included at least two of the following signs: bowel wall thickening (\>4 mm), diverticular inflammation, pericolic fat edema, intramural or pericolic inflammatory mass, intramural fistula. The diagnostic criteria for water soluble contrast enema included segmental luminal narrowing and a tethered mucosa with or without a mass effect or extravasation of contrast and/or the presence of extraluminal air. Exclusion criteria Patients with inflammatory bowel disease, irritable bowel syndrome, colorectal cancer or diseases precluding adequate follow up, were excluded from the study. Treatment Patients were treated conservatively (antibiotics, I.V. nutrition, CT/US guided abscess drainage) or surgically according to the local policy of each center. Follow up Follow up was carried out according to local policy. The following data were collected: persistence or recurrence of chronic symptoms attributable to complicated diverticular disease, new episodes of AD, new hospital admissions for AD, type of treatment and outcome. Recurrence was defined as a new episode of AD requiring hospitalization that occurred at least 2 months after complete resolution of the index episode which resulted in inclusion in the study. If surgery was performed, the timing, type of procedure, Hinchey stage and complications were recorded. Data collection A standardized flow sheet was used to collect data on medical history, diagnostic work up, type of treatment and follow up to create a dedicated database. Gender, age, date of hospital admission and discharge, diagnosis on admission and discharge, co-morbidities (diabetes mellitus, cardiovascular disease, atherosclerosis, liver or renal failure), symptoms experienced before admission and their duration, history of diverticulosis, previous episodes of AD, laboratory tests, and treatment performed were recorded. Where surgery was performed, the date and type of procedure, the operative findings including Hinchey's classification (16) and details of the operation (incision, extension of resection, type of anastomosis, covering stoma, drains), pathology report, and postoperative complications occurring within 30 days, were all recorded. End points The primary endpoint was to assess the rate of recurrence of AD requiring hospitalization during the follow-up period. Additional endpoints were to assess the risks of emergency surgery, stoma and disease-related mortality during the follow up.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Jan 1996
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 1996
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 1999
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 1999
CompletedFirst Submitted
Initial submission to the registry
January 12, 2011
CompletedFirst Posted
Study publicly available on registry
January 13, 2011
CompletedJanuary 24, 2011
December 1, 2010
3.9 years
January 12, 2011
January 21, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
to assess the rate of recurrence of acute diverticulitis requiring hospitalization during the follow-up period
10 years
Secondary Outcomes (1)
to assess the risks of emergency surgery, stoma and disease-related mortality during the follow up
10 years
Study Arms (1)
Acute Diverticulitis
Interventions
Eligibility Criteria
All consecutive patients with left sided acute diverticulitis diagnosed clinically by the presence of abdominal pain, associated with leukocytosis (\>11x109) and/or fever \>38°C, confirmed by imaging (CT scan, ultrasonography, water soluble contrast enema) either alone or in combination and/or by operative findings
You may qualify if:
- All consecutive patients with left sided acute diverticulitis diagnosed clinically by the presence of:
- abdominal pain,
- leukocytosis (\>11x109)
- fever \>38°C and confirmed by imaging (CT scan, ultrasonography, water soluble contrast enema)
- The CT criteria for the diagnosis included at least one of:
- a localized thickening (≥4 mm) of the colonic wall
- signs of inflammation of the pericolic fat
- abscess
- extraluminal air
- extraluminal contrast
- The ultrasound criteria included at least two of:
- bowel wall thickening (\>4 mm)
- diverticular inflammation
- pericolic fat edema
- intramural or pericolic inflammatory mass
- +7 more criteria
You may not qualify if:
- inflammatory bowel disease
- irritable bowel syndrome
- colorectal cancer
- diseases precluding adequate follow up
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Surgery - Galliera Hospital
Genova, 16128, Italy
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
January 12, 2011
First Posted
January 13, 2011
Study Start
January 1, 1996
Primary Completion
December 1, 1999
Study Completion
December 1, 1999
Last Updated
January 24, 2011
Record last verified: 2010-12