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Combined Endoscopic & Radiologic Intervention For Management Of Acute Perforated Peptic Ulcer

Combined Endoscopic & Radiologic Intervention For Management Of Acute Perforated Peptic Ulcer : A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05051683
Acronym
ppu
Enrollment
100
Registered
2021-09-21
Start date
2019-12-30
Completion date
2021-09-01
Last updated
2021-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdomen, Acute

Keywords

perforated peptic ulcer

Brief 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.

Detailed 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).

Interventions

PROCEDUREcombined endoscopic & radiologic intervention for management of acute perforated peptic ulcer

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.

Sponsors

Zagazig University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model 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 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.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Any patients with acute perforated peptic ulcer manifestations . \_ age over 18 years.

Exclusion criteria

* Patients presented with septic shock . \_ age below 18 years

Design outcomes

Primary

MeasureTime frameDescription
incidence of complications after combined endoscopic & radiologic interventionwithin one week after the endoscopyincidence of complications after combined endoscopic & radiologic intervention

Secondary

MeasureTime frameDescription
incidence of mortality after combined endoscopic & radiologic interventionwithin one month after the endoscopyincidence of mortality after combined endoscopic & radiologic intervention

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026