Liver DamagePhase 3HEMOPATCHNCT02769754
Effectiveness of the Use of the New Hemostatic Patch Hemopatch ® in Patients Undergoing Surgical Liver Resection
A Phase 3 study testing Hemopatch in people with Liver Damage and Surgery, run by Instituto de Investigacion Sanitaria La Fe at 1 site in Spain.
Trial summary
This prospective randomized study aims to determine the influence of the use of local hemostatic on the incidence of local complications derived from the edge of transection: biliary fistula or bleeding, after scheduled hepatic resection. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Liver Damage, Surgery
- What is being tested?
- Hemopatch
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 250 participants
- Where
- 1 siteSpain
- Study dates
- May 2016to May 2019
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Scheduled major or minor liver resection surgery by laparotomy approach.
- Age>18
- They have given their written consent voluntarily after having offered the possibility of their participation in the study.
Who cannot join
- Pregnancy and lactation
- Patients with urgent surgery
- Concomitant surgery of another organ
- Gallbladder or biliary-enteric anastomosis associated.
- ALPPS surgery (stands for Associating Liver Partition and Portal vein Ligation for Staged hepatectomy).
- Patients with liver transplantation history.
Show all 9Show fewer
- Patients with previous liver trauma.
- Patients with congenital haematological disease involving clotting factors alteration.
- Patients with known hypersensitivity to bovine proteins and brilliant blue colorante (FD\&C Nº1).
Trial locations and contacts
1 site in 1 country.
Spain1 site, 1 recruiting
- Recruiting
Hospital Universitario y Politécnico La Fe
Valencia, 46026
Rafael López-Andújar, 0034961245858, rlopezandujar@telefonica.net
About this study
Official title: Phase III, Randomized, Unblinded, Controlled Clinical Trial for Evaluating the Effectiveness of the Use of the New Hemostatic Patch Hemopatch ® in Patients Undergoing Surgical Liver Resection
This prospective randomized study aims to determine the influence of the use of local hemostatic on the incidence of local complications derived from the edge of transection: biliary fistula or bleeding, after scheduled hepatic resection.
Read the detailed description
Achieving adequate hemostasis is a fundamental prerequisite to successfully perform any surgical procedure, but particularly in cases of visceral abdominal surgery, where a slight bleeding, apparently insignificant, can end in significant bleeding (Haas et al Clinic and Applied thombosis 2006).
Control of intraoperative bleeding is initially performed using traditional techniques such as compression, ligatures, clips, Electrocautery, or clamps. The traditional surgical techniques often fail to prevent bleeding, despite performing a careful and meticulous hemostasis.
The morbidity after elective liver surgery has been reduced in hepatobiliary surgery centers mainly after standardizing anatomical liver resections. These techniques decrease necrosis, bleeding, and the incidence of biliary fistulas (Kraus et al J Am Coll Surg 2005).
Bleeding and biliary fistula are the main determinants of postoperative liver morbidity, with an incidence around 4.2-10% and 4-17% respectively (Yamashita et al Ann Surg 2001; Jin et al World J Gastroenterology 2013).
This complication is difficult to handle especially in patients with cirrhosis or liver cancer, because of reduced platelet and blood coagulation activity (Figueras et al Ann Surg 2007).
Moreover, it is particularly difficult to determine the individual risk of rebleeding or biliary fistula during the intraoperative time.
Many adjuvant surgical hemostatic procedures have been tested in the liver: such as oxidized cellulose, absorbable sponges, fibrillar collagen, and fibrin sealants.
There is an extensive published literature reporting the use of adhesives, Sealants, and topical hemostatics in surgery. There is little doubt that the hemostatic effects of these devices produce a beneficial impact on blood loss. However, there is a wide variation in the literature results. Most of the initial clinical data were obtained in cardiovascular surgery. The only trial that has provided the most significant data in hemostatic efficacy was published by Rousou et al in J Thorac Cardiol South 1999. In this randomized multicenter study, 333 patients that underwent emergency cardiac reoperations were randomized to receive either conventional treatment with fibrinogen or other hemostatic. The 92% of the patients assigned to receive fibrin sealant had a complete hemostasis at 5 minutes, compared with the 12% of those treated with other topical hemostatic.
In clinical practice is difficult to quantify the efficacy of the topical hemostatics on hemostasis. The overall effect of perioperative blood loss can only be inferred indirectly by volume drainage and the number of transfused concentrates (Kraus et al J Am Coll Surg 2005).
The volume of blood loss during liver surgery depends on many factors: systemic coagulation, underlying disease, surgery complexity, surgeon experience, central venous pressure, and local hemodynamics.
Moreover, bile leakages are much harder to identify, define, and particularly to quantify, when compared to bleeding. The biliary system is a low pressure system (less than venous pressure). Animal studies have shown that the use of collagen adhesives is effective for preventing biliary fistulas (Wise et al Am Surg 2002).
In a cohort study of 32 adult patients, in which a right hepatic lobe Split was held, it was compared the use of Tachosil ® versus fibrin glue. The transection area was treated with fibrin glue in 16 patients and with Tachosil ® in the other 16 ones. No differences were observed regarding the need of postoperative transfusion. Nevertheless, the group of patients treated with the fibrin patch showed a significantly lower incidence of bile leakage. Those findings were justified based on the assumption that the use of a fibrin patch, according to its base rich in fibrin, prevents bile leakage, occluding the biliary radicals at the transection (Toti et al Dig Liver Dis. 2010).
The first clinical trial comparing a hemostatic patch (Tachosil ®) versus the standard surgical hemostasis with Argon was published by Frilling et al in 2005 (Frilling et al Langenbecks Arch Surg. 2005). It was observed a reduction in the intraoperative time for hemostasis and less posterior drain in the Tachosil ® group (N = 121).
In 2007, Figueras et al (Figueras et al Ann Surg 2007) published the results of a randomized clinical trial comparing the fibrin glue administration (Tissucol ® + collagen sponge) versus control in 300 patients. The results showed no differences between groups in blood loss, transfusions, and incidence of biliary fistula, and therefore it was concluded that the cessation of the use of fibrin sealant would be a justified saving cost.
In the clinical trial recently published by Moench et al (Langenbecks Arch Surg. 2014) they studied the intraoperative time of hemostasis evaluated at 3 minutes by a non-inferiority design. The collagen hemostatic agent Sangustop ® proved to be as effective as the fibrinogen and thrombin sponge Tachosil ® in times of intraoperative hemostasis (n = 128).
The different results observed among studies may be due to the diversity of the agents evaluated, the poor standardization of the application techniques, and especially by the clinical differences.
Hemopatch® is indicated as a hemostatic device in procedures when the surgical control of bleeding by pressure, ligation, or conventional methods is inefficient or impractical. It consists in a soft, thin, foldable, and flexible collagen patch derived from bovine skin, and NHS-PEG coated (pentaerythritol polyethylene glycol ether tetrasuccinimidil glutarate). The white face, which is applied on the tissue, is covered with a thin layer of NHS-PEG providing a firm adherence to it, thus sealing the bleeding surface and inducing hemostasis at the same time. Because of its flexible structure, the application of Hemopatch ® on the site to achieve hemostasis is easily controlled. The uncoated side is marked with blue squares of a biocompatible dye, to differentiate it from the coated side.
- Conditions
- Liver Damage, Surgery
- Being tested
- Hemopatch, Control
- Keywords
- LIVER, RESECTION, SURGERY
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HemopatchDevice
Hemopatch will be apply once the standard surgical hemostasis is achieved.
ControlOther
No additional treatment will be applied after performing the usual surgical hemostasis.
| Study group | Role | What they receive |
|---|---|---|
| Control | Placebo comparator | In the control group (group A) no additional treatment will be applied after performing the usual surgical hemostasis. Receives: Other: Control |
| Hemopatch | Experimental | Hemopatch will be apply in the treatment group (group B), once the standard surgical hemostasis is achieved Receives: Device: Hemopatch |
What is being measured
The primary outcome is the main question the study is designed to answer.
Bleeding
Bleeding is defined as the fall of > 3 g/dl of hemoglobin in the postoperative as compared to the baseline value after the operation (the hemoglobin level immediately after surgery) and/or any postoperative transfusion of red blood cells packages because of hemoglobin drop and/or the need for reoperation to stop the bleeding (e.g., embolization or re- laparotomy).
Measured: Day 0 to day 30 (+-10 days)
Presence of Biliary Fistula
Biliary fistula is defined as the presence of high bilirubin levels (Bilirubin> 3x in serum level measured at the same time) in the abdominal drainage, being included the need for interventional radiology due to biliary collection or a re-laparotomy due to biliary fistula (Brooke-Smith et al HPB 2015).
Measured: Day 0 to day 30 (+-10 days)
Secondary outcomes (27)
Age
Measured: Preoperative
Body Mass Index (BMI)
Measured: Preoperative
Gender
Measured: Preoperative
Medical history (heart disease, lung disease, cirrhosis)
Measured: Preoperative
Hypertension
Measured: Preoperative
Dyslipemia
Measured: Preoperative
Tobacco
Measured: Preoperative
Alcohol
Measured: Preoperative
Characteristics of liver disease
Characteristics of liver disease: benign-malignant (source)
Measured: Preoperative
Type of surgery
Type of surgery:Liver resection: major/minor.
Measured: On surgery
Type of surgery
Type of surgery: Number of resected segments/type
Measured: On surgery
Type of surgery
Type of surgery: Number-size of hemostatic patches used as well as their location
Measured: On surgery
Need of transfusion
concentrates number
Measured: Day 0 to day 30 (+-10 days)
Need of transfusion
blood / plasma / platelet d. intraoperative / postoperative e. blood / plasma / platelet f. concentrates number
Measured: Day 0 to day 30 (+-10 days)
Incidence of re-interventions
Incidence of re-interventions (No / Yes / Number / match)
Measured: 30 days after surgery
Postoperative liver failure
Measured: Day 5 after surgery
Infection or wound dehiscence
Measured: 30 days after surgery
Interventional radiology procedures
Number of interventional radiology procedures needed and findings
Measured: 30 days after surgery
Mortality
Mortality p.o. (defined as the existence of the event within 30 days p.o.).
Measured: 30 days after surgery
Hospital stay (HS)
Hospital stay (HS) defined as number of days from the preoperative admission to discharge.
Measured: Up to 30 days after surgery
Readmissions
Readmissions (No / Yes / number of days of re-entry / Cause).
Measured: From hospital discharge to 30 days after.
Preoperative Chemotherapy Administration
Up to 30 days after surgery
Measured: Preoperative
immunosuppressive therapy
Measured: Preoperative
Diuresis
Measured: Up to 30 days after surgery
Temperature
Measured: Up to 30 days after surgery
Blood preassure
Measured: Up to 30 days after surgery
Concomitant medication
Measured: Up to 30 days after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 May 2016 (estimated)
- Study startMay 2016
- Primary completionFeb 2019 (estimated)
- Study completionMay 2019 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Liver DamageStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 250 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Instituto de Investigacion Sanitaria La Fe
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Rafael López-Andújar, Principal investigator, Instituto de Investigación Sanitaria La Fe
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02769754
- Sponsor's protocol ID
- HEMOPATCH
- Acronym
- HEMOPATCH
- Status last verified
- May 2016
- First submitted
- 6 May 2016
- Last updated
- 15 Feb 2018
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- Undecided
Publications
Robledo AB, Montalva Oron EM, Seller AN, Ibanez JM, Sanz AH, Mizrahi DC, Orbis Castellanos FJ, Andujar RL. Clinical evidence on the use of Hemopatch(R) in reducing bleeding and biliary fistula after liver resection: Prospective randomized study in planned surgery. Cir Esp (Engl Ed). 2026 Feb;104(2):800270. doi: 10.1016/j.cireng.2025.800270. Epub 2025 Dec 17.
PubMed 41418882
Study at a glance
From the registry record, last updated by the sponsor on 15 Feb 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase III, Randomized, Unblinded, Controlled Clinical Trial for Evaluating the Effectiveness of the Use of the New Hemostatic Patch Hemopatch ® in Patients Undergoing Surgical Liver Resection
- ClinicalTrials.gov ID
- NCT02769754
- Acronym / sponsor ID
- HEMOPATCH / HEMOPATCH
- Conditions
- Liver Damage, Surgery
- Keywords
- LIVER, RESECTION, SURGERY
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 250 participants (estimated)
- Lead sponsor
- Instituto de Investigacion Sanitaria La FeUniversity, hospital or other
- Study start
- May 2016
- Primary completion
- Feb 2019 (estimated)
- Study completion
- May 2019 (estimated)
- First posted
- 12 May 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This prospective randomized study aims to determine the influence of the use of local hemostatic on the incidence of local complications derived from the edge of transection: biliary fistula or bleeding, after scheduled hepatic resection.
Detailed description
Achieving adequate hemostasis is a fundamental prerequisite to successfully perform any surgical procedure, but particularly in cases of visceral abdominal surgery, where a slight bleeding, apparently insignificant, can end in significant bleeding (Haas et al Clinic and Applied thombosis 2006).
Control of intraoperative bleeding is initially performed using traditional techniques such as compression, ligatures, clips, Electrocautery, or clamps. The traditional surgical techniques often fail to prevent bleeding, despite performing a careful and meticulous hemostasis.
The morbidity after elective liver surgery has been reduced in hepatobiliary surgery centers mainly after standardizing anatomical liver resections. These techniques decrease necrosis, bleeding, and the incidence of biliary fistulas (Kraus et al J Am Coll Surg 2005).
Bleeding and biliary fistula are the main determinants of postoperative liver morbidity, with an incidence around 4.2-10% and 4-17% respectively (Yamashita et al Ann Surg 2001; Jin et al World J Gastroenterology 2013).
This complication is difficult to handle especially in patients with cirrhosis or liver cancer, because of reduced platelet and blood coagulation activity (Figueras et al Ann Surg 2007).
Moreover, it is particularly difficult to determine the individual risk of rebleeding or biliary fistula during the intraoperative time.
Many adjuvant surgical hemostatic procedures have been tested in the liver: such as oxidized cellulose, absorbable sponges, fibrillar collagen, and fibrin sealants.
There is an extensive published literature reporting the use of adhesives, Sealants, and topical hemostatics in surgery. There is little doubt that the hemostatic effects of these devices produce a beneficial impact on blood loss. However, there is a wide variation in the literature results. Most of the initial clinical data were obtained in cardiovascular surgery. The only trial that has provided the most significant data in hemostatic efficacy was published by Rousou et al in J Thorac Cardiol South 1999. In this randomized multicenter study, 333 patients that underwent emergency cardiac reoperations were randomized to receive either conventional treatment with fibrinogen or other hemostatic. The 92% of the patients assigned to receive fibrin sealant had a complete hemostasis at 5 minutes, compared with the 12% of those treated with other topical hemostatic.
In clinical practice is difficult to quantify the efficacy of the topical hemostatics on hemostasis. The overall effect of perioperative blood loss can only be inferred indirectly by volume drainage and the number of transfused concentrates (Kraus et al J Am Coll Surg 2005).
The volume of blood loss during liver surgery depends on many factors: systemic coagulation, underlying disease, surgery complexity, surgeon experience, central venous pressure, and local hemodynamics.
Moreover, bile leakages are much harder to identify, define, and particularly to quantify, when compared to bleeding. The biliary system is a low pressure system (less than venous pressure). Animal studies have shown that the use of collagen adhesives is effective for preventing biliary fistulas (Wise et al Am Surg 2002).
In a cohort study of 32 adult patients, in which a right hepatic lobe Split was held, it was compared the use of Tachosil ® versus fibrin glue. The transection area was treated with fibrin glue in 16 patients and with Tachosil ® in the other 16 ones. No differences were observed regarding the need of postoperative transfusion. Nevertheless, the group of patients treated with the fibrin patch showed a significantly lower incidence of bile leakage. Those findings were justified based on the assumption that the use of a fibrin patch, according to its base rich in fibrin, prevents bile leakage, occluding the biliary radicals at the transection (Toti et al Dig Liver Dis. 2010).
The first clinical trial comparing a hemostatic patch (Tachosil ®) versus the standard surgical hemostasis with Argon was published by Frilling et al in 2005 (Frilling et al Langenbecks Arch Surg. 2005). It was observed a reduction in the intraoperative time for hemostasis and less posterior drain in the Tachosil ® group (N = 121).
In 2007, Figueras et al (Figueras et al Ann Surg 2007) published the results of a randomized clinical trial comparing the fibrin glue administration (Tissucol ® + collagen sponge) versus control in 300 patients. The results showed no differences between groups in blood loss, transfusions, and incidence of biliary fistula, and therefore it was concluded that the cessation of the use of fibrin sealant would be a justified saving cost.
In the clinical trial recently published by Moench et al (Langenbecks Arch Surg. 2014) they studied the intraoperative time of hemostasis evaluated at 3 minutes by a non-inferiority design. The collagen hemostatic agent Sangustop ® proved to be as effective as the fibrinogen and thrombin sponge Tachosil ® in times of intraoperative hemostasis (n = 128).
The different results observed among studies may be due to the diversity of the agents evaluated, the poor standardization of the application techniques, and especially by the clinical differences.
Hemopatch® is indicated as a hemostatic device in procedures when the surgical control of bleeding by pressure, ligation, or conventional methods is inefficient or impractical. It consists in a soft, thin, foldable, and flexible collagen patch derived from bovine skin, and NHS-PEG coated (pentaerythritol polyethylene glycol ether tetrasuccinimidil glutarate). The white face, which is applied on the tissue, is covered with a thin layer of NHS-PEG providing a firm adherence to it, thus sealing the bleeding surface and inducing hemostasis at the same time. Because of its flexible structure, the application of Hemopatch ® on the site to achieve hemostasis is easily controlled. The uncoated side is marked with blue squares of a biocompatible dye, to differentiate it from the coated side.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control | Placebo comparator | Other: ControlIn the control group (group A) no additional treatment will be applied after performing the usual surgical hemostasis. |
| Hemopatch | Experimental | Device: HemopatchHemopatch will be apply in the treatment group (group B), once the standard surgical hemostasis is achieved |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Scheduled major or minor liver resection surgery by laparotomy approach.
- Age>18
- They have given their written consent voluntarily after having offered the possibility of their participation in the study.
Key exclusion criteria (9 listed)
- Pregnancy and lactation
- Patients with urgent surgery
- Concomitant surgery of another organ
- Gallbladder or biliary-enteric anastomosis associated.
- ALPPS surgery (stands for Associating Liver Partition and Portal vein Ligation for Staged hepatectomy).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| HemopatchHemopatch will be apply once the standard surgical hemostasis is achieved. | Device | Hemopatch |
| ControlNo additional treatment will be applied after performing the usual surgical hemostasis. | Other | Control |
Primary outcome
Bleeding
Time frame: Day 0 to day 30 (+-10 days)
Bleeding is defined as the fall of > 3 g/dl of hemoglobin in the postoperative as compared to the baseline value after the operation (the hemoglobin level immediately after surgery) and/or any postoperative transfusion of red blood cells packages because of hemoglobin drop and/or the need for reoperation to stop the bleeding (e.g., embolization or re- laparotomy).
Presence of Biliary Fistula
Time frame: Day 0 to day 30 (+-10 days)
Biliary fistula is defined as the presence of high bilirubin levels (Bilirubin> 3x in serum level measured at the same time) in the abdominal drainage, being included the need for interventional radiology due to biliary collection or a re-laparotomy due to biliary fistula (Brooke-Smith et al HPB 2015).
27 secondary outcomes
Age
Time frame: Preoperative
Body Mass Index (BMI)
Time frame: Preoperative
Gender
Time frame: Preoperative
Medical history (heart disease, lung disease, cirrhosis)
Time frame: Preoperative
Hypertension
Time frame: Preoperative
Dyslipemia
Time frame: Preoperative
Tobacco
Time frame: Preoperative
Alcohol
Time frame: Preoperative
Characteristics of liver disease
Time frame: Preoperative
Type of surgery
Time frame: On surgery
Type of surgery
Time frame: On surgery
Type of surgery
Time frame: On surgery
Need of transfusion
Time frame: Day 0 to day 30 (+-10 days)
Need of transfusion
Time frame: Day 0 to day 30 (+-10 days)
Incidence of re-interventions
Time frame: 30 days after surgery
Postoperative liver failure
Time frame: Day 5 after surgery
Infection or wound dehiscence
Time frame: 30 days after surgery
Interventional radiology procedures
Time frame: 30 days after surgery
Mortality
Time frame: 30 days after surgery
Hospital stay (HS)
Time frame: Up to 30 days after surgery
Readmissions
Time frame: From hospital discharge to 30 days after.
Preoperative Chemotherapy Administration
Time frame: Preoperative
immunosuppressive therapy
Time frame: Preoperative
Diuresis
Time frame: Up to 30 days after surgery
Temperature
Time frame: Up to 30 days after surgery
Blood preassure
Time frame: Up to 30 days after surgery
Concomitant medication
Time frame: Up to 30 days after surgery
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Feb 2018.
- Derived from this study: PubMed 41418882Robledo AB, Montalva Oron EM, Seller AN, Ibanez JM, Sanz AH, Mizrahi DC, Orbis Castellanos FJ, Andujar RL. Clinical evidence on the use of Hemopatch(R) in reducing bleeding and biliary fistula after liver resection: Prospective randomized study in planned surgery. Cir Esp (Engl Ed). 2026 Feb;104(2):800270. doi: 10.1016/j.cireng.2025.800270. Epub 2025 Dec 17.
- Individual participant dataSharing planned: Undecided
Related trials for Liver Damage
Recruiting
Dietary Intervention Study on Liver Health in Young Adults
Liver Health
Recruiting
Identification of Anti-HIF 1alpha Autoantibodies in Patients With Anorexia Nervosa and Characterization of Their Pathogenic Potential in Undernutrition-associated Hepatic Cytolysis
Hepatic Cytolysis
RecruitingPhase 4
Comparative Evaluation of the Performance of Different Thromboplastin Reagents on Prothrombin Time in Situations of Isolated Extrinsic Pathway Factor Deficiency or Liver Damage
Hemorrhagic Disorders
RecruitingPhase 1
A Study of Eloralintide (LY3841136) in Participants With Different Levels of Liver Damage and in Participants With Healthy Livers.
Hepatic Insufficiency
RecruitingObservational study
Drug-Induced Liver Injury (DILI) Network Retrospective
Drug Induced Liver Injury
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rafael López-Andújar principal investigator
Instituto de Investigación Sanitaria La Fe
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Hemopatch in people with Liver Damage and Surgery, run by Instituto de Investigacion Sanitaria La Fe at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 15 Feb 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Elena García (0034961246611, investigacion_clinica@iislafe.es), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Bleeding (time frame: Day 0 to day 30 (+-10 days)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02769754, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Feb 2018.