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A Single-Center Retrospective Study of Clamp Test-Guided Biliary Management in Patients with Cholangiocarcinoma After Percutaneous Transhepatic Biliary Drainage Combined with Hepatic Arterial Infusion Chemotherapy (CCA-CLAMP2606)

A Single-Center Retrospective Study of Clamp Test-Guided Biliary Management in Patients with Cholangiocarcinoma After Percutaneous Transhepatic Biliary Drainage Combined with Hepatic Arterial Infusion Chemotherapy (CCA-CLAMP2606)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129357
Enrollment
Unknown
Registered
2026-08-04
Start date
2026-08-04
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perihilar cholangiocarcinoma

Interventions

Negative clamp test group & Positive clamp test group:None

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=18 years, male or female, ECOG performance status score of 0–1, Child-Pugh class A or B; 2.Diagnosis of hilar cholangiocarcinoma confirmed by pathology, cytology, or by imaging findings combined with clinical data; 3.Received PTCD for malignant obstructive jaundice; 4.Received HAIC after PTCD, with the specific regimen based on real-world clinical treatment records at the study center; 5.Rchieved jaundice relief after treatment and underwent a clamp test according to clinical evaluation; 6.Clamp test-related data and follow-up information were complete or substantially complete;

Exclusion criteria

Exclusion criteria: 1.History of biliary stent placement or biliary stent placement shortly after PTCD combined with HAIC; 2.Previous diagnosis of any other malignancy, except basal cell carcinoma or squamous cell carcinoma of the skin treated with curative intent, or cervical carcinoma in situ; 3.No actual clamp test performed or clamp test results unavailable for evaluation; 4.Missing key outcome data, such as survival status, date of last follow-up, or records of biliary reintervention; 5.Any other conditions deemed unsuitable for inclusion in the analysis by the investigators.

Design outcomes

Secondary

MeasureTime frame
Duration of jaundice relief;Adverse events related to clamping and tube removal;The rate of no drainage and no jaundice for 6/12/24 months;overall survival;Rate of clamping;Jaundice-free and drainage-free duration;Rate of biliary re-intervention;

Primary

MeasureTime frame
Negative rate of the clamping test;Rate of tube removal;

Countries

China

Contacts

Public ContactXiaodong Wang

Beijing Cancer Hospital

tigat@126.com+86 10 88196330

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026