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Application of optical coherence tomography in preoperative evaluation of perihilar cholangiocarcinoma

Application of optical coherence tomography in preoperative evaluation of perihilar cholangiocarcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091695
Enrollment
Unknown
Registered
2024-11-01
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

peihilar cholangiocarcinoma

Interventions

Sponsors

Tsinghua University Affiliated Beijing Tsinghua Changgung Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age range: 18-80 years old; (2) Visited our hospital due to obstructive jaundice and suspected perihilar cholangiocarcinoma, requiring PTCD jaundice reduction treatment or other obstructive jaundice patients requiring PTCD jaundice reduction treatment; (3) Applicable and willing to cooperate with endoscopic OCT examination by the subjects; (4) The patient plans to undergo subsequent surgical treatment; (5) Surgical resection of hilar cholangiocarcinoma is the initial treatment; (6) Willing to comply with research procedures and willing to sign a written informed consent form; (7) There is complete clinical and pathological data available.

Exclusion criteria

Exclusion criteria: (1) Preoperative diagnosis of perihilar cholangiocarcinoma in patients who have not undergone radical surgical treatment; (2) Patients who only undergo exploratory laparotomy or palliative surgery; (3) Patients with recurrent hilar cholangiocarcinoma who undergo reoperation after surgery; (4) Subjects who are contraindicated for PTCD surgery; (5) Pregnant or lactating women; (6) Other researchers believe that patients who are not suitable to participate in the study, such as some patients with hilar cholangiocarcinoma who have high-risk infectious factors.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;Accuracy;

Secondary

MeasureTime frame
positive predictive value;negative predictive value;

Countries

China

Contacts

Public ContactXiang Canhong

Tsinghua University Affiliated Beijing Tsinghua Changgung Hospital

xcha01114@btch.edu.cn+86 133 7017 6344

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026