Safety and Efficacy of Prophylactic Arterial Embolization in the Treatment of Angiography-negative Acute Upper Gastrointestinal Bleeding

Guided by clinical problems, this study focused on the problems encountered in clinical practice, with the interventional treatment of emergency gastrointestinal bleeding as the breakthrough point, and focused on the dilemma of treatment selection for patients with negative angiography in gastrointestinal bleeding. At present, there is no report on relevant clinical and basic research on the selection of treatment strategies for patients with negative ANVUGIB angiography. Whether prophylactic arterial embolization can benefit patients and whether it can reduce mortality is an urgent clinical problem to be solved.

Study Overview

• Status: Recruiting
• Conditions: Acute Gastrointestinal Bleeding
• Intervention / Treatment: Procedure: embolization

Detailed Description

1. Research subjects Patients who were admitted to our hospital from January 2021 to December 2023 and underwent interventional therapy for acute non-variceal upper gastrointestinal bleeding and were negative on angiography were selected.

   Once the subjects signed the informed consent and participated in the screening, the subjects who met all the following inclusion criteria according to the experimental protocol and did not meet any of the exclusion criteria were eligible for screening.

2. Study endpoints 1) The primary endpoint: postoperative rebleeding rate. 2) Secondary endpoints: hemoglobin, hematocrit, blood transfusion volume, complication rate, mortality, surgical intervention rate.
3. In/Out Criteria 1) Inclusion criteria: (1) Age: 18~75 years old (including 18 years old and 75 years old); (2) Bleeding of gastric or duodenal ulcers that have failed endoscopic therapy; (3) Anastomotic bleeding after gastrointestinal anastomosis; (4) Anastomotic bleeding after cholangioenterostomy; (5) Bleeding after ERCP; (6) There were no indirect signs of contrast agent spillage and bleeding in angiography.

2) Exclusion criteria:

(1) Age: <18 years old or >75 years old; (2) Rupture and bleeding of gastric fundus esophageal varices; (3) Active bleeding can be seen on angiography; (4) Upper gastrointestinal bleeding caused by other causes other than the inclusion criteria; (5) Unexplained upper gastrointestinal bleeding; (6) Those who have undergone interventional therapy in the past; (7) Allergy to iodine-containing contrast agents; (8) Uncorrectable coagulation dysfunction and uncontrolled systemic infection; (9) There is functional failure of important organs (heart, liver, kidney, etc.); (10) History of gastrointestinal radiotherapy in the past 1 year; (11) Those who are not expected to complete the follow-up; (12) Expected survival shorter than 6 months. 3) Elimination criteria

1. After enrollment, it is found that the subjects do not meet the inclusion criteria or meet the exclusion criteria;
2. Other diseases or conditions occurred during the trial, which, as judged by the investigator, significantly affected the evaluation of clinical status and research endpoints;
3. Those whose treatment was interrupted due to various reasons or whose case records were incomplete, were determined by the investigators to be unevaluable.

4) Exit/Abort:

1. The subject himself or his legal representative requests to withdraw from the research;
2. Lost to follow-up;
3. DEATH. For all cases of rejection, withdrawal/discontinuation, the reason for rejection, withdrawal/discontinuation must be recorded on the case report form and subject medical records.

4. Interventional treatment process

1. Preoperative preparation: perfect electrocardiogram, gastroscope (optional), chest X-ray/chest CT (optional), enhanced abdominal CT (optional), blood routine, biochemistry, coagulation function, stool routine + occult blood, eight items before surgery etc.; signed informed consent for interventional therapy.
2. Angiography: (1) Prepare the skin at the puncture site, sterilize and lay down sheets; (2) Determine the puncture point: routinely choose the right femoral artery, or the left femoral artery or radial artery, (3) Lidocaine Anesthetize the puncture point, puncture and introduce the 4-5F arterial sheath; (4) Conventional angiography: celiac artery (5-7ml/s, total amount of contrast agent 25-35ml, 300 psi), superior mesenteric artery (5-7ml/s, Total volume of contrast agent 25-35ml, 300 psi). (5) Superselective angiography: superselective angiography of the blood supply artery in the lesion area is performed according to the cause of bleeding, the lesion site determined by endoscopic or enhanced CT, and the flow rate of contrast agent, the duration of angiography and the pressure are determined according to the diameter of the blood vessel.
3. Group processing:

(1) Control group: After angiography, no embolization was given, the catheter was withdrawn, the vascular sheath was removed, and symptomatic and supportive treatments such as acid suppression, hemostasis, blood transfusion, and fluid replacement were given.

(2) Observation group: Prophylactic arterial embolization was performed for the artery in the blood supply area of the lesion. Embolization material: gelatin sponge particles are recommended, and micro-steel ring can be used as an auxiliary if necessary; postoperatively, according to the condition, symptomatic acid suppression, hemostasis, blood transfusion, and fluid replacement were given. and supportive care.

Indications for blood transfusion: (1) systolic blood pressure < 90 mmHg, or a decrease of > 30 mmHg from baseline systolic blood pressure; (2) hemoglobin < 70 g/L, hematocrit < 25%; (3) increased heart rate (> 120 times/min).

4. Postoperative treatment: (1) Monitoring vital signs; (2) On the 1st, 7th, and 14th days after operation, and in January and March respectively, test blood routine, coagulation function, liver and kidney function, stool routine + occult blood, etc.; ( 3) Observe the bleeding situation; (4) Observe and record adverse reactions.

6. Angiographic findings

1. Positive signs of bleeding: contrast agent spillage, pseudoaneurysm, irregular arterial stenosis/truncation.
2. Negative signs of bleeding: the shape of blood vessels is obviously abnormal, and the above positive signs are not present on angiography.

6. Efficacy evaluation Technical success: Successful embolization of the target arterial vessel. Technical failure: The target artery was not successfully embolized. Clinical success: no more active bleeding within 1 month after surgery, or significant reduction in bleeding volume, no need for blood transfusion therapy Bleeding stopped: (1) bleeding from gastric tube or abdominal drainage tube stopped; (2) the patient's symptoms improved, heart rate and blood pressure were stable; (3) urine output > 0.5 ml/kg/h. Active bleeding: (1) bleeding from gastric tube or abdominal drainage tube; (2) increased frequency of hematemesis or melena, bright red vomit or dark red blood in stool, or active bowel sounds; (3) rapid infusion Blood transfusion, the performance of peripheral circulatory failure did not improve significantly, or although it temporarily improved and then deteriorated, the central venous pressure still fluctuated, stabilized and then decreased again; (4) red blood cell count, hemoglobin concentration and hematocrit continued to decline, reticulum The red blood cell count continued to increase; (5) the blood urea nitrogen continued or increased again when the fluid and urine volume were sufficient.

7. Safety evaluation:

1. Serious complications: require surgical treatment or prolong hospital stay for ≥2 weeks.
2. Mild complications: no surgical treatment or prolonged hospital stay is required for less than 2 weeks.

Recording of complications: from the time the subjects signed the informed consent, until the subjects completed or withdrew from the trial. All adverse events that occurred during the trial must be recorded on a case report form. The contents of the records should include: the occurrence time, severity, duration, measures taken and outcomes of adverse events.

Technical difficulties: For the judgment of negative angiography, it is generally accepted that when the bleeding rate is lower than 15ml/min, the bleeding point cannot be found by DSA angiography, but it is also related to the pressure of the high-pressure syringe, the diameter of the blood vessel and the experience of the operator.

• Study Type: Interventional
• Enrollment (Anticipated): 60
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Shilong Han, Doctor; Phone Number: 18917683645; Email: hanshilong86@163.com
• Study Contact Backup: Name: Long Pan, Doctor; Phone Number: 18917685712; Email: 18917685712@189.com

Study Locations

• China
  • Shanghai, China
    • Recruiting
    • Shanghai 10th People's Hospital
    • Contact: Long Pan; Phone Number: 189 1768 5712

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years to 75 years (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Age: 18~75 years old (including 18 years old and 75 years old);
2. Bleeding of gastric or duodenal ulcers that have failed endoscopic therapy;
3. Anastomotic bleeding after gastrointestinal anastomosis;
4. Anastomotic bleeding after cholangioenterostomy;
5. Bleeding after ERCP;
6. There were no indirect signs of contrast agent spillage and bleeding in angiography.

Exclusion Criteria:

1. Age: <18 years old or >75 years old;
2. Rupture and bleeding of gastric fundus esophageal varices;
3. Active bleeding can be seen on angiography;
4. Upper gastrointestinal bleeding caused by other causes other than the inclusion criteria;
5. Unexplained upper gastrointestinal bleeding;
6. Those who have undergone interventional therapy in the past;
7. Allergy to iodine-containing contrast agents;
8. Uncorrectable coagulation dysfunction and uncontrolled systemic infection;
9. There is functional failure of important organs (heart, liver, kidney, etc.);
10. History of gastrointestinal radiotherapy in the past 1 year;
11. Those who are not expected to complete the follow-up;
12. Expected survival shorter than 6 months.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Prophylic Embolization; Prophylactic arterial embolization is performed for the artery in the diseased blood supply area. The embolization material: gelatin sponge particles are recommended, and micro-steel ring can be used as an auxiliary if necessary; after operation, symptomatic and supportive treatment such as acid suppression, hemostasis, blood transfusion, and fluid replacement are given according to the condition.	Procedure: embolization; Prophylactic arterial embolization is performed for the artery in the diseased blood supply area. The embolization material: gelatin sponge particles are recommended, and micro-steel ring can be used as an auxiliary if necessary; after operation, symptomatic and supportive treatment such as acid suppression, hemostasis, blood transfusion, and fluid replacement are given according to the condition.
Sham Comparator: Sham Embolization; After the angiography was completed, no embolization was performed, the catheter was withdrawn, the vascular sheath was removed, and symptomatic and supportive treatments such as acid suppression, hemostasis, blood transfusion, and fluid replacement were given.	Procedure: embolization; Prophylactic arterial embolization is performed for the artery in the diseased blood supply area. The embolization material: gelatin sponge particles are recommended, and micro-steel ring can be used as an auxiliary if necessary; after operation, symptomatic and supportive treatment such as acid suppression, hemostasis, blood transfusion, and fluid replacement are given according to the condition.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
postoperative rebleeding rate	No more active bleeding within 1 month after surgery, or the bleeding volume is significantly reduced, and no blood transfusion is required	1 month

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Hemoglobin	Hemoglobin count	1 month
blood transfusion volume	how much blood the patients need	1 month
complication rate	if there are any complications	1 month
mortality	number of patients dead within one month	1 month
surgical intervention rate.	patients need surgery	1 month

Collaborators and Investigators

• Sponsor: Shanghai 10th People's Hospital

Study record dates

Study Major Dates

• Study Start (Anticipated): September 30, 2022
• Primary Completion (Anticipated): December 30, 2023
• Study Completion (Anticipated): December 30, 2023

Study Registration Dates

• First Submitted: September 10, 2022
• First Submitted That Met QC Criteria: September 21, 2022
• First Posted (Actual): September 22, 2022

Study Record Updates

• Last Update Posted (Actual): September 23, 2022
• Last Update Submitted That Met QC Criteria: September 22, 2022
• Last Verified: September 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Digestive System Diseases; Pathologic Processes; Gastrointestinal Diseases; Hemorrhage; Gastrointestinal Hemorrhage
• Other Study ID Numbers: SHSY-IEC-5.0/22K8/P01; 20204Y0167 (Other Grant/Funding Number: Shanghai Municipal Health Commission)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No