Pulmonary Hypertension Trial, Recruiting NCT07176962 Sponsor: Yingbin Liu, MD, PhD, FACS Condition: Pulmonary Hypertension
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Pulmonary Hypertension Trial, Recruiting

NCT07176962
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

People with biliary tract cancer (internal training/validation group):

  • People aged 18 to 80 who have been diagnosed with biliary tract cancer (any stage) confirmed by a pathologist, are generally well enough to carry out basic daily activities, and have blood test results showing the liver, kidneys, and blood counts are within acceptable ranges.

People with other digestive system cancers (comparison group):

  • People aged 18 to 80 who have been diagnosed with a gastrointestinal cancer other than biliary tract cancer — such as liver, stomach, bowel, or pancreatic cancer (any stage) — and are generally well enough to carry out basic daily activities.

People with non-cancerous bile duct or gallbladder conditions (comparison group):

  • People aged 18 to 80 who have been diagnosed with a benign (non-cancerous) condition affecting the gallbladder or bile ducts, such as gallstones, gallbladder polyps, inflammation of the gallbladder, or primary sclerosing cholangitis.

People with suspected biliary tract cancer (external validation group):

  • People aged 18 to 80 whose scans or blood tests strongly suggest biliary tract cancer, and who are already scheduled for surgery or a biopsy to confirm the diagnosis, and whose organ function blood results are within acceptable ranges.

Healthy volunteers (external validation group):

  • People aged 18 to 80 with no cancer history who are able to provide blood samples and give their consent to participate.

All groups require participants to be willing to take part, able to follow the study procedures, and able to provide the required blood samples. Consent may be given by a legally authorised representative if the participant is unable to sign.


Who may not be able to join:

Cancer participants:

  • Women who are pregnant or breastfeeding.
  • People who have had an organ transplant or a bone marrow or stem cell transplant from a donor.
  • People who received a blood transfusion within 7 days before the blood sample is taken.
  • People who received curative cancer treatment within the past 3 years (or are currently undergoing such treatment, in the external validation group).
  • People who have taken anti-cancer drugs within the past 30 days before the blood sample is taken.
  • People with a known bleeding disorder.
  • People with a known autoimmune disease.
  • People who have more than one active cancer at the same time, or more than one primary cancer.
  • For the external validation group: people whose biopsy or surgery confirms a benign (non-cancerous) condition, people who carry known cancer-risk gene variants, or people whose cancer cannot be confirmed within 42 days of the blood sample being taken.
  • For the external validation group: people who have already received any cancer treatment — including surgery, radiotherapy, targeted therapy, or immunotherapy — before the blood sample is taken, or whose biopsy confirms only a pre-cancerous lesion.

Non-cancer participants and healthy volunteers:

  • Women who are pregnant or breastfeeding.
  • People who have had an organ transplant or a bone marrow or stem cell transplant from a donor.
  • People who received a blood transfusion within 7 days before the blood sample is taken.
  • People with any history of cancer.
  • People with a known bleeding disorder or autoimmune disease.
  • People with significant abnormalities found on a routine health check (minor findings such as hepatitis, liver cysts, or small benign lung nodules may not necessarily exclude someone — confirm with trial site).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Yingbin Liu, PhD, RenJi Hospital

Phone: +86 13918803900

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Yingbin Liu, MD, PhD, FACS
Registry
ClinicalTrials.gov
Start date
1 January 2020
Est. completion
21 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Diagnostic performance of the ctDNA methylation model in biliary tract cancer

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov