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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01886248
Other study ID # Antithrombin-III
Secondary ID
Status Active, not recruiting
Phase Phase 2
First received
Last updated
Start date June 2013
Est. completion date August 2021

Study information

Verified date March 2021
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate efficacy and safety of AT-III treatment in patients with hepatic veno-occlusive diseases following hematopoietic stem cell transplantation.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 32
Est. completion date August 2021
Est. primary completion date August 2021
Accepts healthy volunteers No
Gender All
Age group N/A to 65 Years
Eligibility Inclusion Criteria: 1. Patients with hepatic veno-occlusive disease after hematopoietic stem cell transplantation. The following criteria will be used. 1. Two of the following - Serum total bilirubin > 2.0 mg/dL - Hepatomegaly or right upper quadrant pain of liver origin - Unexplained weight gain of>2% over baseline because of fluid accumulation 2. Patients with pathologic diagnosis. 2. Patients with informed consent Exclusion Criteria: 1. Pregnant or nursing women. 2. Malignant or nonmalignant illness that is uncontrolled or whose control may be jeopardized by complications of study therapy. 3. Psychiatric disorder that would preclude compliance. 4. Patients who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study. 5. History of anaphylactic reaction to the study drug

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Freeze-dried Concentrated Human Antithrombin ? 500 IU


Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul Chongno-gu

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary AT-III level before 5th dose of AT-III up to 14 days
Secondary AT-III level before 9th dose up to 14 days
See also
  Status Clinical Trial Phase
No longer available NCT00143546 - Compassionate Use of Defibrotide for Patients With Veno-occlusive Disease of the Liver N/A
Recruiting NCT00563498 - Effects on Glutamine on the Outcome of Allogeneic Bone Marrow Transplant Recipients N/A
Not yet recruiting NCT04168788 - Pharmacogenetic Study of Antimitotic Therapies Involved in Hepatic VOD in Children With Nephroblastoma or ALL N/A
Completed NCT00628498 - Defibrotide for Patients With Hepatic Veno-occlusive Disease: A Treatment IND Study Phase 3
Completed NCT00272948 - Pediatric Trial Investigating the Incidence & Outcome of Veno-Occlusive Disease With the Prophylactic Use of Defibrotide Phase 2/Phase 3
Completed NCT03032016 - European VOD Registry