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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04242979
Other study ID # HA use in liver cirrhosis
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 1, 2020
Est. completion date April 1, 2023

Study information

Verified date January 2020
Source Assiut University
Contact Abdelrahman Salah Abodief, MBBCh
Phone 01003447486
Email abodief.zeid1234@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Due to shortage of local studies of the adherence of physicians to the guidelines for albumin use among patients with liver cirrhosis so this study aims to assess:

1. Physicians' knowledge on the evidence-based indications for HA use supported by the international guidelines;

2. Whether HA is used in clinical conditions not supported by solid scientific evidence;

3. To formulate the evidence-based indications for HA use supported by the international guidelines and to evaluate effect of distributing these evidence-based indications on physicians' knowledge.


Description:

- In the last part of the previous century the increasing knowledge about the cardiovascular abnormalities that occur in advanced cirrhosis led researchers to design prospective randomized clinical trials assessing the effect of exogenous human albumin (HA) based on its well-established capacity to act as plasma-expander.

- Due to the positive results reported by those studies, international guidelines have included the administration of HA among the recommendations for the prevention of post-paracentesis circulatory dysfunction (PPCD) or renal failure induced by spontaneous bacterial peritonitis (SBP), and for the diagnosis and treatment of hepatorenal syndrome (HRS) .

- Indeed, all these complications are characterized by a substantial reduction of effective volemia. However, even in these settings, questions regarding HA dosage and whether or not all patients should be treated remain unanswered .

- It has now become evident that circulatory dysfunction and organ damage in patients with decompensated cirrhosis are related to a chronic state of systemic inflammation and oxidative stress, which can abruptly exacerbate in patients developing acute-on-chronic liver failure (ACLF), a syndrome characterized by extra-hepatic organ failure and poor short-term survival.

- Besides colloid-osmotic power, HA is provided with many biological properties unrelated to the regulation of fluid compartmentalization. Among these, some would assume particular importance in relation to the inflammatory state of decompensated cirrhosis, such as antioxidant and scavenging activities, binding and transport of many endogenous and exogenous substances, and regulation of endothelial function and inflammatory/immunological response .

- Therefore, due to both its oncotic and non-oncotic properties, HA may exert beneficial effects at different steps of the cascade of the pathogenetic events that link circulatory dysfunction to systemic inflammation, providing a novel pathophysiological perspective for the use of HA. In this regard, two nationwide surveys on the use of HA in patients with cirrhosis conducted in the United States and France aiming to assess the adherence to the current AASLD and EASL guidelines respectively, have shown that HA is also prescribed besides the evidence-based indications. Indeed, HA is not rarely employed in non-SBP bacterial infections, severe hyponatremia, and hypoalbuminemia.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1
Est. completion date April 1, 2023
Est. primary completion date April 1, 2022
Accepts healthy volunteers No
Gender All
Age group 26 Years and older
Eligibility Inclusion Criteria:

Gastroenterology physicians in:

- Al-Rajhi Liver Hospital (Tropical Medicine Department, and Internal Medicine, GIT Unit).

- Police Hospital.

- Health Insurance Hospital.

- Assiut Center for Management of HCV.

- El - Shamla Hospital.

- Al-Eman Hospital.

Exclusion Criteria:

- Non gastroenterology physicians

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Questionnaire about albumin use in liver cirrhosis
Permission to carry out the study will be obtained from the Faculty's Ethics Committee. To achieve validity and reliability of the tool. It will be reviewed by two experts in the field of the study and necessary modification will be done. A pilot study will be 10% done to test the clarity and feasibility of developed tool. Each participant involved in the study will be assessed for his or her knowledge using (tool I). Data will be collected by personal interview with participants or via fulfilling online questionnaire taking in consideration data confidentiality. Application of the designed evidence based indications for human albumin use supported by the international guidelines will be done by researcher using (tool II). Evaluate the effect of the designed evidence based indications for human albumin use supported by the international guidelines on physicians' knowledge after 1 month using (tool I) in a random sample of those physicians

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Abdelrahman Salah Eldin Abodief

References & Publications (1)

Caraceni P, Pavesi M, Baldassarre M, Bernardi M, Arroyo V. The use of human albumin in patients with cirrhosis: a European survey. Expert Rev Gastroenterol Hepatol. 2018 Jun;12(6):625-632. doi: 10.1080/17474124.2018.1460203. Epub 2018 Apr 4. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Questionnaire The investigators will know physicians' basic mean knowledge score about human albumin use in validated and non validated indications.
The score will be from (0-2)
1 month
Secondary Questionnaire The investigators will determine the effect of designed evidence based indication for human albumin use supported by the international guidelines on mean knowledge scores of physicians.The score will be from (0-2) 2-3 years
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