Rifamycin SV-MMX® 400 mg b.i.d. vs. Rifamycin SV-MMX® 600 mg t.i.d. vs. Placebo in Acute Uncompli… (NCT01847664) | Clinical Trial Compass
CompletedPhase 2
Rifamycin SV-MMX® 400 mg b.i.d. vs. Rifamycin SV-MMX® 600 mg t.i.d. vs. Placebo in Acute Uncomplicated Diverticulitis
Germany204 participantsStarted 2013-08
Plain-language summary
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.
Who can participate
Age range18 Years – 80 Years
SexALL
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Inclusion criteria
✓. Signed informed consent,
✓. Patient is eligible for out-patient treatment,
✓. Men or women between 18 and 80 years of age,
✓. Diagnosis of left-sided uncomplicated diverticulitis confirmed by ultrasonography (US) and/or computed tomography (CT) according to modified Hinchey classification (stage 1a) or Hansen/Stock classification (stage I/IIa) or Ambrosetti classification (stage mild),
✓. Presence of significant left lower quadrant pain during the last 24 hours before baseline,