- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04746326
Treatment in Right Colon Diverticulitis Patients
February 5, 2021 updated by: Semra Demirli Atici, Tepecik Training and Research Hospital
Operative and Conservative Treatment in Right Colon Diverticulitis Patients
The right colon diverticula, unlike those in the left colon, contain all layers of the colon and is called the true diverticulum.
Perforation is observed less frequently due to its full thickness.
Conservative treatment can be applied unless complications such as abscess formation and free perforation occur.
Unlike the left, right colon diverticulitis has low complications and can be treated conservatively.
The differential diagnosis of right colon diverticulitis should be kept in mind in order to prevent unnecessary surgeries.
Surgical treatment is inevitable in cases such as recurrent diverticulitis, generalized peritonitis, and suspected malignancy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The right colon diverticula, unlike those in the left colon, contain all layers of the colon and is called the true diverticulum.
Perforation is observed less frequently due to its full thickness.
Conservative treatment can be applied unless complications such as abscess formation and free perforation occur.
Here, we aimed to discuss the results of conservative and surgical treatment for right colon diverticulitis in the light of the literature.
150 patients treated for colon diverticulitis between 2015-2020 were retrospectively screened.
Right colon diverticulitis detected incidentally, missing data, and left colon diverticulitis were excluded from the study.
Data of a total of 26 patients were accessed.
Unlike the left, right colon diverticulitis has low complications and can be treated conservatively.
The differential diagnosis of right colon diverticulitis should be kept in mind in order to prevent unnecessary surgeries.
Surgical treatment is inevitable in cases such as recurrent diverticulitis, generalized peritonitis, and suspected malignancy
Study Type
Interventional
Enrollment (Actual)
26
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
İzmir, Turkey, 35180
- Tepecik Training and Research Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- diagnosed with right colon diverticulitis
Exclusion Criteria:
- Left colon diverticulitis
- Right colon diverticulitis detected incidentally
- lacking data
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Conservative treatment
Conservative treatment stopping oral intake, intravenous antibiotic therapy.
|
Conservative treatment was performed in patients who had no generalized peritonitis and perforation.
|
Other: Operative treatment
Operative procedure Right hemicolectomy Wedge resection of cecum Diverticulectomy + appendectomy Diverticulectomy Appendectomy + drainage
|
Surgery was performed in patients who failed conservative treatment.
Surgery was performed in patients who had generalized peritonitis and perforation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Participants with mortality
Time Frame: up to 24 weeks
|
mortality
|
up to 24 weeks
|
Number of Participants with wound infection
Time Frame: up to 24 weeks
|
wound infection
|
up to 24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2020
Primary Completion (Actual)
January 1, 2021
Study Completion (Actual)
January 20, 2021
Study Registration Dates
First Submitted
January 29, 2021
First Submitted That Met QC Criteria
February 5, 2021
First Posted (Actual)
February 9, 2021
Study Record Updates
Last Update Posted (Actual)
February 9, 2021
Last Update Submitted That Met QC Criteria
February 5, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020 / 14-6
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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