Diverticulitis Clinical Trial
Aim: This is a longitudinal cohort study to assess long-term clinical outcome of patients
who were admitted in our institution for a first episode of uncomplicated sigmoid
diverticulitis.
Methods: All patients who were diagnosed with a first episode of sigmoid diverticulitis will
be evaluated for inclusion in the study, pending informed consent. Those patients who have
evidence of complicated diverticulitis (fistula, abscess) will receive a recommendation to
undergo elective sigmoid resection, while those who have a simple attack will be recruited
in the cohort. Follow-up will be performed at yearly intervals through telephone interview
with the patient. The duration of study is expected to last 10 years (2010-2020), with >50
new patients/year, for a total of >500 patients.
Endpoints:
1. the occurrence of a second episode of diverticulitis
2. severity and outcome of recurrent diverticulitis
3. evolution in digestive symptoms and quality of life (QoL)
4. need for subsequent elective or emergency sigmoid resection
Rationale: This study will help in determining the risk/benefit of the current approach for
this common condition, which is to manage patients conservatively with antibiotics and adopt
a wait-and-see attitude. Specifically, the following events will be assessed quantitatively:
- the rate of relapse in an urban community.
- the burden of this common disease on QoL and digestive function
- the percentage of patients who may need emergency surgery
Status | Recruiting |
Enrollment | 500 |
Est. completion date | January 2017 |
Est. primary completion date | January 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
4.2. Inclusion criteria - Informed consent - A first episode of uncomplicated diverticulitis (see definitions), which was documented with CT scan, required hospital admission, and was successfully managed with intravenous antibiotics Or - A first episode of complicated diverticulitis (Hinchey I or II - see definition), requiring CT scan-guided percutaneous drainage, and successfully managed without surgery in a patient either unfit for, or refusing to undergo elective sigmoid resection Exclusion criteria - Age < 18 or > 90 - Associated condition of the colon or rectum (cancer, IBD, polyps) - Patient unable to communicate in French, English or German |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Switzerland | University Hospital Geneva | Geneva |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Geneva |
Switzerland,
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03042091 -
Neomycin and Metronidazole Hydrochloride With or Without Polyethylene Glycol in Reducing Infection in Patients Undergoing Elective Colorectal Surgery
|
Early Phase 1 | |
Completed |
NCT02246361 -
Impact of Six Patient Information Leaflets (PIL) on Doctor Patient Communication
|
Phase 4 | |
Completed |
NCT01476995 -
Prognostic Indicators as Provided by the EPIC ClearView
|
N/A | |
Completed |
NCT01081054 -
Hospitalization or Ambulatory Treatment of Acute Diverticulitis
|
Phase 4 | |
Completed |
NCT00195351 -
Study Comparing Tigecycline Versus Ceftriaxone Sodium Plus Metronidazole in Complicated Intra-abdominal Infection
|
Phase 4 | |
Completed |
NCT03337984 -
Damage Control Surgery in the Treatment of Complicated Diverticulitis
|
||
Recruiting |
NCT06210724 -
FIT in Diverticulitis
|
||
Completed |
NCT01986686 -
Recurrence Following Nonoperative Management of 1st Episode of Hinchey II Diverticulitis
|
N/A | |
Completed |
NCT01477190 -
Spinal Analgesia for Colonic Resection Using an Enhanced Recovery After Surgery (ERAS) Program
|
Phase 1/Phase 2 | |
Completed |
NCT01056913 -
NITI CAR27 (ColonRing) Compression Anastomosis in Colorectal Surgery
|
Phase 4 | |
Completed |
NCT00468455 -
Post-Op Quality of Life After Colorectal Surgery
|
N/A | |
Completed |
NCT00230971 -
Study Comparing Tigecycline Versus Ceftriaxone Sodium Plus Metronidazole in Complicated Intra-abdominal Infection (cIAI)
|
Phase 4 | |
Enrolling by invitation |
NCT03700593 -
Feasibility and Safety of Single Port Robot in Colorectal Procedures
|
||
Recruiting |
NCT04095663 -
Comparison of Surgery and Medicine on the Impact of Diverticulitis (COSMID) Trial
|
N/A | |
Completed |
NCT00545740 -
Prevention of Recurrence of Diverticulitis
|
Phase 3 | |
Recruiting |
NCT01837342 -
Multicenter Study Comparing Morbidity and Quality of Life Associated in the Treatment by Surgical Resection and the Conservative Treatment, After Favorable Evolution of Purulent Peritonitis That Originates From Diverticulitis Treated by Mini-invasive Surgery
|
N/A | |
Completed |
NCT01727388 -
Informativeness to Digital Rectal Examination
|
Phase 3 | |
Completed |
NCT00554099 -
Asacol Acute Diverticulitis(DIVA)Study
|
Phase 2 | |
Completed |
NCT04173182 -
Confocal Laser Endomicrospy in Colonic Diverticular Disease
|
||
Completed |
NCT02200055 -
Using Electrical Bioimpedance Assessments to Estimate Perioperative Total Body Water and Postoperative Fluid Need
|
N/A |