Hartmann vs R/A in Peritonitis by Perforated Diverticulitis

Phase 2

Completed

• Conditions: Peritonitis Caused by Perforated Left-sided Colon Diverticulitis

• Registration Number: NCT01239927
• Lead Sponsor: Ente Ospedaliero Ospedali Galliera

Brief Summary

This prospective randomized trial is to prove the equivalence of primary sigmoid resection with end colostomy(Hartmann)(GROUP A) and primary sigmoid resection and immediate anastomosis with diverting stoma (GROUP B)with regard to morbidity and mortality in patients with peritonitis caused by perforated left-sided colon diverticulitis.

Detailed Description

Not available

Study Timeline

• Study Start: 2000-01
• Status Verified: 2010-07
• Primary Completion: 2010-07
• Study Completion: 2010-07
• Study First Submitted: 2010-11-12
• Study First Submitted QC: 2010-11-12
• Last Update Submitted: 2010-11-12
• Study First Posted: 2010-11-15
• Last Update Posted: 2010-11-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• Intraoperative demonstrated peritonitis caused by perforated left-sided colon diverticulitis

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
30-day mortality and morbidity after emergency surgery	30-day

Secondary Outcome Measures

Name	Time	Method
30-day mortality and morbidity after elective restoration of intestinal transit	30 day

Trial Locations

Locations (1)

Gian Andrea Binda; 🇮🇹 Genova, Italy