The purpose of the trial is to compare the efficacy of Rifamycin SV-MMX® 400 mg b.i.d. vs. Rifamycin SV-MMX® 600 mg t.i.d. vs. placebo in patients with acute uncomplicated diverticulitis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
204
Evangelisches Krankenhaus Kalk
Cologne, North Rhine-Westphalia, Germany
Rate of patients with treatment success at the day 10 visit
Treatment success includes e.g.: * absence of diverticulitis related symptoms * no complications of acute diverticulitis * no hospitalisation due to acute diverticulitis
Time frame: 10 days
First visit with treatment success
Time frame: 10 days
Rate of surgical intervention of acute diverticulitis
Time frame: 10 days
Rate of hospitalisation due to acute diverticulitis
Time frame: 10 days
Rate of occurrence of complicated diverticulitis
Time frame: 10 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.