Fibrosis

12

Review clinical trials related to Fibrosis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Screening and Follow-up in Patients With HIV Infection Combined With Metabolic Associated Fatty Liver Disease

Acquired immunodeficiency syndrome (AIDS) remains a severe global infectious disease, with over 38 million people living with HIV and around 35 million cumulative deaths worldwide by 2023; approximately 1.24 million HIV-positive individuals and 100,000 new infections are reported annually in China. Widespread use of HAART has prolonged HIV patients' survival and reduced AIDS-related mortality, yet non-AIDS comorbidities dominated by chronic liver disorders, particularly metabolic dysfunction-associated fatty liver disease (MAFLD), have become a major challenge in long-term HIV management. Triggered by elevated blood lipids from lifestyle, antiretroviral agents and inherited metabolic factors, MAFLD initiates with hepatic steatosis and may progress to NASH, liver fibrosis, cirrhosis and even hepatocellular carcinoma (HCC) without timely intervention. HIV-positive patients develop more severe MAFLD progression than HIV-negative counterparts; existing biopsy data shows 91% of ART-treated HIV patients have NAFLD, among whom 65% suffer from NASH complicated with liver fibrosis. Fatty liver prevalence keeps rising with younger onset age in China, which highlights the necessity of early screening. Liver biopsy, the historical diagnostic gold standard for liver injury grading, is restricted by invasiveness, bleeding risks and poor reproducibility. Transient elastography (TE), a novel non-invasive ultrasonic technique, quantifies hepatic steatosis via the ultrasound attenuation parameter (UAP) and liver fibrosis via liver stiffness measurement (LSM), and has been validated and guideline-endorsed for multiple chronic liver diseases globally. Published foreign data report 35%, 42% and 22% prevalence of NAFLD, NASH and fibrosis in PLWH, while domestic evidence on HIV-associated MAFLD is limited, especially liver-related discrepancies among varied ART regimens. With the implementation of China's new medical insurance policy, numerous patients are shifting from non-INI regimens to once-daily single-tablet INSTI STR regimens, whose hepatic and lipid impacts remain unclear. This study targets early detection of HIV patients with concomitant fatty liver to optimize management strategies and improve clinical outcomes. Our preliminary cohort at Peking Union Medical College Hospital included 188 virologically suppressed HIV patients on ART, 56.9% (107/188) of whom developed fatty liver (mild:27.1%, moderate:19.7%, severe:10.1%). Liver fibrosis (LSM≥7.3 kPa) was found in 12.8% (24/188) subjects, with 1.1% having advanced cirrhosis, and no significant inter-group difference in fatty liver incidence was noted between INSTI and NNRTI recipients. These findings lay a foundation for early diagnosis and follow-up intervention of metabolic liver disease among HIV-infected populations.

Participants needed: 2,000
Trial details
Biological sex: AllType: ObservationalSponsor: Peking Union Medical College HospitalUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Newly treated or treated AIDS patients; [+2]

Unable to complete the position requirements of ultrasonic examination (lying fl... [+3]

Status: Recruiting

A Study of Mosliciguat in Combination With Inhaled Treprostinil in PH-ILD

This is a Phase 2, open-label, multi-center clinical study to evaluate the safety and tolerability of inhaled mosliciguat in participants with pulmonary hypertension associated with interstitial lung disease (PH-ILD) on a background inhaled treprostinil.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-85Biological sex: AllType: InterventionalSponsor: Pulmovant, Inc.Updated: Apr 22, 2026Locations: 1
Eligibility criteria

Participants willing and able to provide informed consent [+6]

Diagnosis of PH Group 1 (eg. pulmonary arterial hypertension), Group 2 (related... [+5]

Status: Recruiting

Evaluation of the Medical Benefit of Spa Therapy on Fibrosis After Radiotherapy for Breast Cancer or UADT (Upper Aerodigestive Tract) Cancer

FIBROTHERME is a comparative, controlled, randomized, multicenter and simple blinded (investigator) trial. The aim of this study is to evaluate the medical benefit in terms of quality of life on the dermatological sequelae of fibrosis 6 months after a dermatologically oriented spa therapy in patients with severe late reactions affecting the skin and/or soft tissues at least 6 months after radiotherapy for breast cancer or UADT (Upper Aerodigestive Tract) cancer.

Participants needed: 110
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Association Francaise pour la Recherche ThermaleUpdated: Apr 13, 2026Locations: 13
Eligibility criteria

Age ≥ 18 years [+10]

Progressive phase of cancer [+10]

Status: Recruiting

Copper Supplementation in Cirrhosis

End stage liver disease or cirrhosis is a major cause of mortality in the United States and the world. Other than targeting the underlying cause, such as alcohol cessation and antiviral therapy, very few medical treatments can change the natural history of cirrhosis. Malnutrition is one of the few potentially modifiable factors that have been associated with cirrhosis severity and poor prognosis. The transition metal copper (Cu) is an essential trace metal that must be acquired from diet. Its metabolism is primarily regulated by the liver in its role as a master regulator of nutrients. In 2019, the investigators reported that Cu deficiency defined by below normal serum or liver concentrations occurred in a wide range of liver disorders and was associated with a severe disease phenotype. Improvement in liver function was observed in 2 of the 3 patients who received Cu supplementation. In 2023, the investigators conducted a longitudinal cohort study utilizing clinical, serum and liver explant tissue data from 183 cirrhosis patients. The investigators showed that Cu deficiency was associated with 2-fold higher infection rate and a more than 3-fold increase in the risk of death compared to patients with normal Cu status. These preliminary findings and the well-established importance of Cu in human health prompted the investigators to design the current pilot randomized, placebo-controlled, crossover trial to determine the effect of Cu supplementation on Cu dependent biochemical changes, patient safety and patient reported outcomes in cirrhosis.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of WashingtonUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Adult patients age 18 or older with confirmed diagnosis of cirrhosis based on cl... [+2]

Patients with Wilson disease, cholestatic liver diseases including primary bilia... [+7]

Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

Dispositioned to radiotherapy with prescribed dose to unilateral or bilateral ne... [+16]

Active liver disease (Child-Pugh class B-C), cirrhosis, nor active alcoholism. [+9]

Status: Recruiting

Diaphragmatic Function as a Biomarker

Dyspnea is among the most common symptoms in patients with respiratory diseases such as Asthma, chronic obstructive pulmonary disease (COPD), Fibrosis, and Pulmonary Hypertension. However, the pathophysiology and underlying mechanisms of dyspnea in patients with respiratory diseases are still poorly understood. Diaphragm dysfunction might be highly prevalent in patients with dyspnea and respiratory diseases. The association of diaphragm function and potential prognostic significance in patients with respiratory diseases has not yet been investigated.

Participants needed: 800
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: RWTH Aachen UniversityUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

patient has one of the following lung diseases: COPD, bronchial asthma, pulmonar... [+4]

BMI > 35 [+9]

Status: Recruiting

Reversing External-beam Radiotherapy-associated Fibrosis Syndrome: an Interventional Bayesian Adaptive Randomized-controlled Orphan Drug Platform Trial for Orodental Sequelae (Reverse-fibrose)

To find out if adding medication can help treat or prevent lymphedema and/or fibrosis related to radiation therapy, in survivors of head and neck cancer. Researchers will compare these drugs to find the most effective therapy for preventing or limiting these side effects.

Participants needed: 250
Trial details
Phase: Phase 2Biological sex: FemaleType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Prior history of head and neck cancer with no active disease. [+10]

Active liver disease (Child-Pugh class B-C), cirrhosis, nor active alcoholism. [+9]

Status: Recruiting

Blood Collection Biorepository for Liver Disease Research

The purpose of establishing a biorepository is to provide high quality specimens (serum, plasma, buffy coat and liver tissue) for future researchers who are studying the effects that fatty liver and viral diseases have on the liver.

Participants needed: 1,000
Trial details
Age: 7+Biological sex: AllType: ObservationalSponsor: State University of New York at BuffaloUpdated: Aug 27, 2025Locations: 1Duration: 1 Day
Eligibility criteria

This protocol is to establish a biobank of blood samples from individuals with o... [+1]

Vulnerable populations such as adults unable to consent, infants, pregnant women...

Status: Recruiting

The Gastric Bypass Stent System as a Treatment for Hepatic Fibrosis in Obese Patients in European Region

The Gastric Bypass Stent System is intended to be used in weight loss treatment for obesity and holds potential as a non-invasive technique for managing hepatic fibrosis. This pilot, prospective, single-arm, clinical investigation aims to evaluate the safety and performance of the Gastric Bypass Stent System for hepatic fibrosis treatment in Europe. This clinical investigation and the ongoing clinical investigation (Protocol number: BL-RD08-040) will be used to evaluate the safety and performance of the investigational device for the intended use.

Participants needed: 10
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: MDCECRO LLCUpdated: May 8, 2025Locations: 2
Eligibility criteria

Age 18-65 years. [+36]

Status: Recruiting

Screening At-risk Populations for Hepatic Fibrosis With Non-invasive Markers

Prospective screening study at Odense University Hospital to assess the effect of transient elastography and other serum and imaging markers of liver fibrosis to detect advanced fibrosis (Kleiner Fibrosis score F3-F4) in patients at risk of non-alcoholic fatty liver disease, alcoholic fatty liver disease, with a control group of participants recruited from the general population.

Participants needed: 6,500
Trial details
Age: 30-75Biological sex: AllType: InterventionalSponsor: Maja ThieleUpdated: Sep 1, 2022Locations: 1
Eligibility criteria

Age 30-75 years (except the general population, which should be aged 40-75) [+5]

Evidence of decompensated liver disease, defined by clinically obvious ascites,... [+7]

Status: Not yet recruiting

THE FRENCH NATIONAL NAFLD COHORT (FRench pAtients With MEtabolic Steatosis)

The main objective of this cohort study is to determine genetic, clinical biologic and metabolic factors associated with patient heterogeneity in regards to severity of NAFLD at diagnosis as well as during the clinical course. * at diagnosis, with the aim to better characterize patients of different severity and improve our understanding of clinical and histological heterogeneity at diagnosis * during the clinical course to better understand and predict disease progression in terms notably of fibrosis progression and progression to cirrhosis

Participants needed: 900
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Jun 14, 2021
Eligibility criteria

Age ≥18 years [+3]

Refusal or inability (lack of capacity) to give informed consent. [+10]

Status: Recruiting

Fibro-inflammatory Progression From Acute to Chronic Pancreatitis

Observational prospective study evaluating the developement of chronic pancreatitis based on imaging modalities as well as biochemical markers of inflammation, fibrosis and oxidative stress.

Participants needed: 150
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Copenhagen University Hospital, HvidovreUpdated: Apr 8, 2020Locations: 3
Eligibility criteria

Patients with CP (N=50) of any aetiology except gallstone induced CP: CP will be... [+2]