Clinical Trials Logo

Clinical Trial Summary

The investigators included all patients who were developed acute perforated peptic ulcer manifestations and were admitted to our hospital between December 2019 to August 2021. The study was approved by the research and Ethics committee of our university and performed in accordance with the code of ethics of the world medical association (Declaration of Helsinki) for studies involving humans. A written informed consent was obtained from all participants. The sample size was calculated using open Epi program using the following data ; confidence interval 95% , power of test 80% , ratio of unexposed/exposed 1, percent of patients with successful management of acute perforated peptic ulcer by surgical intervention 90% and those with successful management by endoscopy 99% , odds ratio 99%, and risk ratio 2 , so the calculated sample size equal 100 patients divided into two equal groups. Group (1) included 50 patients managed by combined endoscopic & radiologic intervention , group (2) included 50 patients managed by surgery.


Clinical Trial Description

The investigators included all patients who were developed acute perforated peptic ulcer manifestations and were admitted to our hospital between December 2019 to August 2021. The study was approved by the research and Ethics committee of our university and performed in accordance with the code of ethics of the world medical association (Declaration of Helsinki) for studies involving humans. A written informed consent was obtained from all participants. The sample size was calculated using open Epi program using the following data ; confidence interval 95% , power of test 80% , ratio of unexposed/exposed 1, percent of patients with successful management of acute perforated peptic ulcer by surgical intervention 90% and those with successful management by endoscopy 99% , odds ratio 99%, and risk ratio 2 , so the calculated sample size equal 100 patients divided into two equal groups. Group (1) included 50 patients managed by combined endoscopic & radiologic intervention , group (2) included 50 patients managed by surgery. Any patients with acute perforated peptic ulcer manifestations and age over 18 years were included. Patients presented with septic shock and age below 18 years were excluded. Perioperative measures: In this prospective randomized controlled trial , all patients were subjected to the followings: patients were selected by randomization method , Full history taking , Complete physical examination , laboratory investigations ( complete blood picture , liver and kidney functions , coagulation profile ) , radiological investigations ( chest x- ray erect , abdominal & pelvic u/s ). Surgical techniques : Traditional surgical exploration and Graham omental patch repair with abdominal lavage either open or laparoscopy was done for group (2). For group (1) endoscopic management using stent , clipping and sewing combined with radiologic interventional drainage was used. For duodenal ulcer only metallic stent was used due to narrow space while for gastric ulcer either stent , clipping and sewing were used due to capacious space. Metallic stent: Upper GI endoscopy ( Model GIF - 2TH180; Olympus , Tokyo, Japan) was done , allowing through it stent placement. The endoscopy was passed beyond the site of perforation , a guide wire was passed through the endoscopy into the proximal part of the jejunum and a partially covered duodenal stent ( Hanaro, MI-tech Korea) was advanced and released over the wire ( Jagwire ; Boston Scientific , Marlborough , M , USA) to cover the perforation site. Attention was taken to place the oral part of the stent above the pylorus and the covered part of the stent at site of perforation. At same time of stent placement a radiologic interventional team worked and drainage was done & 2 intra-peritoneal tube drains were inserted one was placed sub-hepatic another was placed in the pelvis. During postoperative day one a methylene blue test was done . and blue color was observed in the drain. Stent was removed 3 weeks later and site of perforation was observed . if there was any sings of remaining perforation a new stent was placed for another 3 weeks. Endoscopic clips: Clips are used to approximate the tissue surrounding the defect to effect closure. Standard clips should be deployed perpendicular to the long axis of the defect. If needed, multiple clips can be placed sequentially, starting at either edge of a defect and meeting at the center. Currently available through-the-scope clips achieve superficial tissue apposition engaging the mucosa and submucosa (with 1.2-mm-wide and 6-mm-long arms capable of an approximately 12-mm grasp), and have been used in conjunction with thermal ablation or mechanical scraping of the tissue around the edges of the defect to achieve a more resilient seal. The Over-the-Scope Clip (Ovesco Endoscopic AG, Tubingen, Germany) is a nitinol clip placed on a cap at the endoscope tip . Unlike clips inserted through the endoscope, the OVESCO can perform full-thickness apposition. At same time a radiologic interventional team worked and drainage was done & 2 intra-peritoneal tube drains were inserted one was placed sub-hepatic another was placed in the pelvis. During postoperative day one a methylene blue test was done . and blue color was observed in the drain. Sewing: The Stomaphy X suturing system (Endo Gastric Solutions, Redmond, WA) and the Apollo Over Stitch (Apollo Endo surgery, Austin, TX), which creates full-thickness plications , has shown early success . At same time a radiologic interventional team worked and drainage was done & 2 intra-peritoneal tube drains were inserted one was placed sub-hepatic another was placed in the pelvis. During postoperative day one a methylene blue test was done . and blue color was observed in the drain. Follow up after surgery and discharge from the hospital: The investigators examined the patients clinically, made routine laboratory investigations , and for group (1) upper GI endoscopy at 2 weeks later. Statistical analysis: The collected data were analyzed by computer using Statistical Package of Social Services version 22 (SPSS), Data were represented in tables and graphs, Continuous Quantitative variables e.g. age were expressed as the mean ± SD & (range), and categorical qualitative variables were expressed as absolute frequencies (number) & relative frequencies (percentage). Suitable statistical tests of significance were used after checked for normality. Categorical data were cross tabulated and analyzed by the Chi-square test or Fisher's Exact Test; Continuous data were evaluated by student t- test. The results were considered statistically significant when the significant probability was less than 0.05 (P < 0.05). P-value < 0.001 was considered highly statistically significant (HS), and P-value ≥ 0.05 was considered statistically insignificant (NS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05051683
Study type Interventional
Source Zagazig University
Contact
Status Completed
Phase N/A
Start date December 30, 2019
Completion date September 1, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT04602429 - Children's Acute Surgical Abdomen Programme
Recruiting NCT03309423 - Is Venous to Arterial Conversion (v-TAC) of Blood Gas Reliable in Critical Ill Patients in the ICU? N/A
Completed NCT02980081 - Abdominal Plain X-ray in the Emergency Departement N/A
Suspended NCT04887480 - Direct Resuscitation of the Open Peritoneum N/A
Completed NCT02582307 - Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children Phase 3
Active, not recruiting NCT04681508 - MINS, AKI and Pulmonary Pathology in Patients Undergoing Acute Abdominal Surgery N/A
Completed NCT05933837 - Troponin I Level and Mortality in Acute Abdominal Surgery
Recruiting NCT03015233 - Acute Abdominal Pain: Evaluation of Lactate Value as Predictive Factor of Surgical Issue N/A
Not yet recruiting NCT06160778 - Intravenous Ketorolac Vs. Morphine In Children With Acute Abdominal Pain Phase 3
Completed NCT05623176 - Clinical Outcomes and Equality in Healthcare for Emergency General Surgery Patients Undergoing Emergency Laparotomy
Completed NCT02047812 - The Hospital Volume Relationship in Emergency Laparotomy Outcomes N/A
Completed NCT02017977 - Geographic Influences on Emergency Laparotomy Outcomes N/A
Completed NCT04176432 - Survival After Emergency Laparotomy in Octogenarians
Completed NCT01538745 - Low Dose Ketamine (LDK) Versus Morphine for Acute Pain Control in the Emergency Department Phase 4
Completed NCT05992961 - The Effects of Troponin I Surveillance Among Patients Undergoing Acute High-risk Abdominal Surgery
Terminated NCT01110382 - A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections Phase 3
Not yet recruiting NCT06008509 - POCUS for Gastric Emptying in Emergency Surgery N/A
Recruiting NCT05910567 - A Research Study of Abdominal Ultrasound (FAST) in Children With Blunt Torso Trauma N/A