Acute Diverticulitis Clinical Trial
Official title:
Multicentre Controlled, Randomized Clinical Trial to Compare the Efficacy and Safety of Ambulatory Treatment of Mild Acute Diverticulitis Without Antibiotics With the Standard Treatment With Antibiotics
Verified date | May 2020 |
Source | Corporacion Parc Tauli |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Patients with mild acute diverticulitis (modified Neff 0 grade), following the inclusion criteria and giving informed consent, will be included in the study protocol and will be randomly assigned to one of the treatment arms: symptomatic treatment with NSAID plus antibiotic vs symptomatic treatment with NSAID only. They will be followed-up at 48 hours, 7 days, 30 days and 3 months from the onset of the episode.
Status | Completed |
Enrollment | 480 |
Est. completion date | April 1, 2020 |
Est. primary completion date | January 12, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Patient's written informed consent. Adequate cognitive capacity. - Adequate family support - No acute diverticulitis episode in the last 3 months - mNeff 0 acute diverticulitis (abdominal computed tomography scan) - No antibiotic treatment in the last 2 weeks - Immunocompetence* - No significant comorbidities** - Good oral tolerance - Good symptom control - Maximum one of the following SIRS criteria (* T>38 ºC or <36ºC, L>12,000 or <4000/uL, HR>90 bpm, RR<20 rpm) or CRP>15 mg/dL Exclusion Criteria: - Women in pregnancy or breastfeeding - Age <18 years or > 80 years. - Absence of the patient's written informed consent. Inadequate cognitive capacity. - Inadequate family support - Acute diverticulitis episode in the last 3 months - Moderate acute diverticulitis (mNeff grade I or upper) - Antibiotic treatment in the last 2 weeks - Inflammatory bowel disease - Immunodepression* - Presence of significant comorbidities** - Bad oral tolerance - Poor symptom control - More than one of the following SIRS criteria (* T>38 ºC or <36ºC, L>12,000 or <4000/uL, HR>90 bpm, RR<20 rpm) or CRP>15 mg/dL (*) Immunocompetence is the absence and immunodepression is the presence of any of the following: active neoplastic disease/hematologic malignancy/HIV with low CD4+ count/long-term corticosteroid treatment/immunosuppressant therapy/transplant/splenectomy/genetic immunodeficiency. (**) We consider significant comorbidities any of the following: poorly controlled diabetes mellitus (HbA1>7mg/dl), cardiologic event in the last 3 months, decompensation of hepatopathy in the last 3 months, renal chronic insufficiency in dialysis programme. |
Country | Name | City | State |
---|---|---|---|
Spain | Corporació Sanitària Parc Taulí | Sabadell | Barcelona |
Lead Sponsor | Collaborator |
---|---|
Corporacion Parc Tauli |
Spain,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Readmission ratio | Primary outcome is to determine if, in mild acute diverticulitis, the treatment without antibiotic is not-inferior to the traditional treatment with antibiotic considering readmission ratio. | 3 months | |
Secondary | Reconsultation ratio | The analysis of the differences between groups, in case there are, in relation to number and reason for reconsultation | 3 months | |
Secondary | Reason for reconsultation | The analysis of the differences between groups, in case there are, in relation to number and reason for reconsultation | 3 months | |
Secondary | Reason for readmission | The analysis of the differences between groups, in case there are, in relation to reason for readmission (bad symptoms control, radiologic progression, analysis worsening) | 3 months | |
Secondary | Pain control | The analysis of the differences between groups, in case there are, in relation to pain control (analogic visual scale), during follow-up. | 48 hours, 7 days, 1 month, 3 months | |
Secondary | Complications | Description of the complications in both groups (perforation, abscess) and its treatment (percutaneous drainage, emergency surgery, broad spectrum antibiotics) | 3 months |
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