Clinical Trials Directory

Trials / Completed

CompletedNCT01620671

Fast-track Surgery for Perforated Peptic Ulcers

The Feasibility of Fast-track Surgery for Perforated Peptic Ulcers. A Prospective Randomized Clinical Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
61 (actual)
Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The concept of "enhanced recovery after surgery" has become increasingly popular in elective abdominal surgeries. Yet, the role of this concept has not been described in emergency procedures. Therefore, this study aimed to investigate the feasibility of fast-track surgery in patients with perforated peptic ulcer.

Detailed description

The study is designed as a randomized, controlled clinical study. The patients with a preoperative diagnosis of perforated peptic ulcer will be recruited for the study. Among those, the patients with a definitive diagnosis of perforated peptic ulcer confirmed by surgical exploration will be included. The patients will be randomized according to their protocol number given automatically by the registration system of the hospital during admission. The patients who have an odd protocol number will have conventional surgical protocol, and those who have an even protocol number will have fast-track surgery protocol. The conventional surgical protocol for perforated peptic ulcers is composed of regular general anesthesia, postoperative pain control by intravenous analgesics, removal of nasogastric tube by the end of 48th postoperative hour, initiation of oral intake after clinical signs of active bowel movement is observed. Fast-track surgery protocol, however, is composed of general anesthesia with short-acting agents and the use of regional anesthesia if possible, removal of nasogastric tube during recovery from anesthesia, aggressive pain control, initiation of oral intake by the end of 48th postoperative hour. All of the patients will be scheduled for control gastroscopy in the end of six weeks after surgery. Primary end-point is the morbidity and mortality rate. Secondary end-points are length of hospital stay, readmission rate, endoscopic findings in control gastroscopy.

Conditions

Interventions

TypeNameDescription
PROCEDURESurgical repair of perforated peptic ulcerPerforated peptic ulcer located in the stomach and the duodenum will be repaired by either primary repair or omentoplasty.
PROCEDURESurgical repair of perforated peptic ulcerPerforated peptic ulcer located in the stomach and the duodenum will be repaired by either primary repair or omentoplasty.

Timeline

Start date
2012-05-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2012-06-15
Last updated
2013-01-23

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT01620671. Inclusion in this directory is not an endorsement.