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CLINICAL STUDY · NCT07265843

Fibrinogen in Liver Transplant

RecruitingPhase 4Interventional

Sponsored by Trauma Hemostatis and Oxygenation Research (THOR) Network

Condition
Liver Transplant Surgery
Study locations
1 reported site
Study updated
19 Oct 2026
Source
ClinicalTrials.gov

Overall study status is shown above. Individual hospitals may have a different recruitment status.

THE STUDY

About this study

The study is a prospective, multi-centered, unblinded, randomized controlled pilot study. The primary objective is to compare functional hemostatic capacity of two approved products Intercept Fibrinogen Complex (IFC) to Standard Cryoprecipitate Antihemophilic Factor (AHF) for liver transplant patients with bleeding and hypofibrinogenemia to determine impact of earlier access to a concentrated source of fibrinogen in a goal-directed manner.
Full official title
Fibrinogen in Liver Transplant Subjects (FITS)
Detailed description
Fibrinogen is an important factor for hemostasis and when it is deficient or dysfunctional replacing it will improve hemostasis and reduce bleeding. Observational data indicates the use of cryoprecipitate as a source of fibrinogen may reduce bleeding and improve outcomes in patients with severe bleeding. Liver transplant patients often become hypofibrinogenemic and may benefit from early goal directed use of cryoprecipitate or IFC. IFC can be more readily available since it can be stored at room temperature compared to cryoprecipitate which requires thawing. As a result, IFC can be immediately available when indicated compared to the delay in administration of cryoprecipitate due to the need for it to be thawed. This trial will compare clinical outcomes for subjects randomized to either cryoprecipitate or IFC in bleeding liver transplant patients with reduced fibrinogen function.

There is no data comparing outcomes for subjects receiving IFC or cryoprecipitate in any patient population.

The rationale for this trial is to compare IFC to cryoprecipitate (cryo) to assist with the design of a future definitive multicenter trial. Potential advantages of IFC are that since it is stored at room temperature it can be made immediately available whereas with cryo the delay in treatment can be 30 to 40 min due to the need to thaw it from a frozen state. The reduced time to treatment of bleeding may improve outcomes with the use of IFC compared to cryo. In vitro data indicates similar hemostatic function between IFC and Cryo. IFC is pathogen reduced cryoprecipitate. The pathogen reduction methods are licensed for IFC and there has been no safety concerns regarding its use at the centers that are currently using it as their standard product (unpublished).

PARTICIPATION

Who may participate

Minimum age
18 Years
Maximum age
Not reported
Sex eligibility
All sexes
Healthy volunteers
Not accepted

Only the study team can confirm eligibility. The registry criteria below are not a medical recommendation.

Full inclusion and exclusion criteria
Inclusion Criteria:

* 18 years of age or older
* Scheduled to undergo cadaveric liver transplant
* Meets at least one of the following criteria: Baseline fibrinogen \<200 mg/dL or clinically significant visoelastic testing
* Meets any one of the following criteria: Alcoholic cirrhosis, Metabolic dysfunction associated steatohepatitis (MASH) (previously known as Nonalcoholic Steatohepatitis (NASH)), HCV infection

Exclusion Criteria:

* Living related donor transplant,
* Known prothrombotic disorder,
* Patient objection to blood transfusion,
* Known severe allergic reaction to plasma-based products,
* IgA deficiency with known hypersensitivity reaction to plasma,
* Hepatocellular/cholangio carcinoma,
* Primary biliary fibrosis
* Active bleeding prior to the operation

NEAR YOU

Study locations worldwide

1 site

Check the individual site’s status and contact the listed study team for current availability.

WHAT IS BEING STUDIED

Treatments and study groups

Interventions

Intercept Fibrinogen Complex (IFC)Biological
INTERCEPT Fibrinogen Complex is a pathogen-reduced cryoprecipitated fibrinogen complex derived from human plasma. It contains fibrinogen, Factor XIII, and von Willebrand factor to achieve stable clot formation and restore hemostasis. Recently approved by the US Food and Drug Administration, it is used for the treatment of bleeding associated with fibrinogen deficiency.

Study groups: Intercept Fibrinogen Complex (IFC)

Cryoprecipitate Antihemophilic Factor (AHF)Biological
Cryoprecipitate Antihemophilic Factor (AHF), also known as cryo, is a frozen blood product prepared from blood plasma. It is used for fibrinogen supplementation, particularly for hypofibrinogenemia fibrinogen, anemia associated with bleeding or congenital deficiency.

Study groups: Standard Antihemophilic Factor (AHF)

Study groups

Standard Antihemophilic Factor (AHF)Active comparator
AHF is the standard of care fibrinogen product often used in liver transplant cases. The procedures to use AHF include requesting the order of this product and then waiting for the product to be thawed for use, which can take approximately 10-15 minutes. Subjects assigned to this group will receive all standard of care procedures, including the use of AHF if required during their scheduled surgery.

Interventions: Biological: Cryoprecipitate Antihemophilic Factor (AHF)

Intercept Fibrinogen Complex (IFC)Active comparator
IFC is an approved fibrinogen product that is not typically stored in the OR for liver transplant cases. Subjects assigned to this group will receive standard of care procedures, with the addition of IFC being readily available in their designated OR to eliminate any delay if they are to require the use of a fibrinogen product.

Interventions: Biological: Intercept Fibrinogen Complex (IFC)

RESEARCH DETAILS

Study design

Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Study model
Parallel
Masking
None (open label)
Enrolment
60 participants · Estimated

Study model details

Prospective, multi-center, unblinded, randomized controlled study.

Masking details

N/A unblinded

TIMELINE & MEASURES

Dates and outcomes

Study started
21 May 2026 · Actual
Primary completion
1 Mar 2028 · Estimated
Study completion
1 Mar 2028 · Estimated
First registered
5 Dec 2025 · Actual
Last registry update
19 Oct 2026 · Actual
Status last verified
Oct 2026
Primary outcomes (1)

Amount of blood products (24-hours) [Time Frame: 24-hours after initial blood product administration]

The amount of blood products (mL) administered will be collected at the 24-hour timepoint per intervention group and reported as the mean (mL).

Time frame: 24-hour

Secondary outcomes (3)

Change in Visoelastic parameters [Time Frame: pre-intervention through 24 hours post intervention]

Change in Visoelastic parameters, in particular the % change in the alpha angle will be calculated for each study participant and the effect size of the differences in the change, and 95% confidence interval.

Time frame: pre intervention through 24 hours post intervention

Costs of blood products [Time Frame: 24 hours]

The costs (USD) of blood products used per intervention group will be collected 24 hours post-surgery and reported as the mean (USD).

Time frame: 24 hours post-surgery

Costs of IV hemostatic agents [Time Frame: 24 hours]

The costs (USD) of IV hemostatic agents used per intervention group will be collected 24 hours post-surgery and reported as the mean (USD).

Time frame: 24 hours post-surgery

STUDY TEAM

Sponsor and contacts

Lead sponsor
Trauma Hemostatis and Oxygenation Research (THOR) Network
Sponsor type
Other
Collaborators
Not reported
Organisation study ID
FITS

Central study contacts

Meghan Huff Research Nurse, BSNContactPhone: 6185789309Email: mhuff@pitt.edu

Contacts are provided by the registry for study enquiries. Do not use these details for marketing or promotions.

FURTHER READING

Results, documents and references

No results are posted in this registry record

This does not mean the study has no findings. Results may not yet have been submitted or published here.

No study documents are listed in this record.

Source: ClinicalTrials.gov · Data fetched 20 Oct 2026, 15:52 GMT+0530

Registry data timestamp: 2026-10-19T09:00:04

Registry content is reformatted for readability; original study text is not rewritten. Missing information is labelled “Not reported”. Records are supplied by study sponsors or investigators and can change.

ClinicalTrials.gov does not endorse PharmaBharat. Listing a study does not mean it has been evaluated or approved by a government agency. Information is for research awareness and is not medical advice. Data source terms · Registry disclaimer