N-butyl-2-cyanoacrylate, Iso-amyl-2-cyanoacrylate and Hypertonic Glucose With 72% Chromated Glycerin in Gastric Varices
NCT ID: NCT02330731
Last Updated: 2015-01-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
90 participants
INTERVENTIONAL
2012-01-31
2012-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
METHODS: Ninety patients with gastric varices presented to Endoscopy Unit of Ain Shams University Hospital were included. They were randomly allocated into three groups; each group included 30 patients treated with intravariceal sclerosant injections in biweekly sessions till complete obturation of gastric varices; Group I (n-butyl-2-cyanoacrylate; Histoacryl®), Group II (iso-amyl-2-cyanoacrylate; Amcrylate®) and Group III (mixture of 72% chromated glycerin; Scleremo® with glucose solution 25%). All the procedures were done electively without active bleeding. Recruited patients were followed up for 3 months.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
EUS-guided Obturation of High Risk Gastric Varices Versus Standard Endoscopic Treatment
NCT04222127
N-Butyl-2-Cyanoacrylate Injection Versus Band Ligation for Gastric Variceal Hemorrhage
NCT00292331
Endoscopic Injection Sclerotherapy Versus N-butyl-2-cyanoacrylate Injection
NCT03388125
Balloon-occluded Retrograde Transvenous Obliteration for Gastric Variceal Rebleeding
NCT06106971
Primary Prophylaxis of Gastric Variceal Bleed
NCT02468180
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Patients are randomly allocated into three groups; each group includes 30 patients who will be treated with sclerosant injections in biweekly sessions till complete obturation of gastric varices, with follow up for 3 months:
* Group I (Histoacryl® Group),
* Group II (Amcrylate® Group) and
* Group III (Scleremo® with Glucose 25% Group). The three groups are matching as regards age, gender, cause of liver cirrhosis (viral hepatitis B or C), Child score and endoscopic findings (including number, grade of EV and size of GV).
* Tools of the study:
All included patients will be subjected to:
1. Complete clinical evaluation.
2. Laboratory investigations: CBC, liver profile, viral markers (HBs Ag, HB core Ab, HCV Ab) by ELISA technique.
3. Child classification according to the modified Child Pugh's criteria \[13\].
4. Abdominal ultrasonography: liver and spleen size, portal vein diameter and ascites.
5. Upper gastrointestinal endoscopy: using Pentax video endoscope EG 3440. Esophageal varices are classified according to their size at the gastroesophageal junction into 4 grades according to Westaby et al. \[14\].
Gastric varices are classified into: gastro-esophageal varices (GEV) and isolated gastric varices (IGV) according to Sarin et al. \[15\].
6. Therapeutic interventions:
The intravariceal technique of injection is done according to Soehendra et al. \[16\].
Histoacryl® is diluted as 0.5 ml histoacryl: 0.8 ml lipidol as a contrast agent to dilute the adhesive material to fill the whole varix and to prevent rapid hardening and obstruction of the needle. The mixture is injected slowly to minimize the risk of embolization followed by injection of 2 ml of distilled water. The first ml of water is injected to push the material into the varix and the second ml is injected during withdrawal of the needle to prevent its obstruction \[8\].
Amcrylate® is injected slowly followed by injection of 2 ml distilled water without mixing with any other substances \[17\].
Scleremo® is mixed with glucose 25% in a ratio of 1:1. The mixture is injected very slowly and with the waiting for moments inside the variceal lumen after injection to give enough time for the sclerosing material to be in contact with the vessel wall that helps haemostasis. There is no need for distilled water injection \[11\].
Informed consent was obtained from all included patients and the study protocol was approved from the ethical guidelines committee.
All the procedures are done electively without active bleeding. The primary end point of this study is the obturation of gastric varices. The secondary endpoint is the occurrence of bleeding whether from the puncture site during or immediately after injection or delayed (in-hospital or after discharge) and mortality.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
N-butyl-2-cyanoacrylate
injection sclerotherapy for gastric varices
injection sclerotherapy for gastric varices
The intravariceal technique of injection
iso-amyl-2-cyanoacrylate
injection sclerotherapy for gastric varices
injection sclerotherapy for gastric varices
The intravariceal technique of injection
72% chromated glycerin
injection sclerotherapy for gastric varices
injection sclerotherapy for gastric varices
The intravariceal technique of injection
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
injection sclerotherapy for gastric varices
The intravariceal technique of injection
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
25 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Sara Abdelhakam
Dr
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Reda Elwakil, MD
Role: PRINCIPAL_INVESTIGATOR
Professor
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
482
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.