Clinical trials

4

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Condition / disease
Location
Status: Not yet recruiting

Fighting the Fear of Cancer Recurrence in Cancer Survivors: A Pilot Study on the Effectiveness of Metacognitive Therapy

This study aims to evaluate the effectiveness of metacognitive therapy (MCT) in reducing fear of cancer recurrence (FCR) among cancer survivors. With advances in cancer treatment, more patients are surviving cancer. However, many survivors continue to experience fear of cancer recurrence, which can affect their emotional well-being, quality of life, and ability to return to normal daily activities. In this study, participants will receive a structured psychological intervention adapted from the ConquerFear program. This program has been modified to better fit local cultural needs. Participants will be randomly assigned to receive either metacognitive therapy or relaxation therapy. The study will compare the effects of these interventions on reducing fear of cancer recurrence, as well as their impact on emotional distress and quality of life. The results of this study may help develop effective psychological treatments to support cancer survivors in managing fear of recurrence and improving overall well-being.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Koo Foundation Sun Yat-Sen Cancer CenterUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

Age 18 years or older. [+3]

Individuals with severe psychiatric disorders. [+1]

Status: Recruiting

Hepatic IA Therapy in Stage B or Limited Stage C Hepatoma (HCC)

Intra-arterial (IA) therapy is generally used to treat HCC tumors that are too extensive to excise or treat with potentially curative local therapy. IA therapy takes advantage of the fact that the blood supply of HCC comes predominantly from the hepatic artery compared with the surrounding normal liver which is predominantly supplied by portal venous blood. The intent is to deprive the HCC of its blood supply, leading to the death of the tumor. Traditionally, various methods have been used to block the HCC blood supply, but improvements are needed. This study will investigate a new agent designed in the laboratory to block only tumor blood vessels, not blood vessels in the normal liver.

Participants needed: 43
Trial details
Phase: Early Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Koo Foundation Sun Yat-Sen Cancer CenterUpdated: Mar 6, 2025Locations: 4
Eligibility criteria

Age ≥ 18 years [+17]

Eligible for transplantation by Milan criteria (Protocol Appendix 3) or potentia... [+16]

Status: Recruiting

Ga-68-FAPI-46 PET for CRC Recurrence Detection in Elevated CEA

This single-center, phase II clinical trial investigates the diagnostic efficacy of Ga-68-FAPI-46 PET scans in detecting colorectal cancer (CRC) recurrence during post-treatment surveillance, particularly in patients with elevated serum carcinoembryonic antigen (CEA). The study compares the sensitivity, specificity, and accuracy of Ga-68-FAPI-46 PET with the conventional F-18-FDG PET scans, aiming to enhance recurrence detection in CRC patients who underwent curative surgery. Thirty participants will be enrolled and monitored through imaging studies and clinical follow-up.

Participants needed: 30
Trial details
Age: 20-100Biological sex: AllType: InterventionalSponsor: Koo Foundation Sun Yat-Sen Cancer CenterUpdated: Jan 22, 2025Locations: 1
Eligibility criteria

Age ≥ 20 years old [+5]

pregnant woman and breastfeeding women [+6]

Status: Recruiting

Ga-68-CXCR4 PET/CT in Indolent B-cell Lymphoma

This study explores the efficacy of Ga-68-PentixaFor PET/CT in detecting, assessing treatment response, and monitoring the risk of aggressiveness in indolent B-cell lymphoma. The background introduces CXCR4 and discusses its role in cancer research. Currently, FDG-PET is the primary imaging tool for lymphoma staging, but it lacks diagnostic accuracy for low-grade lymphomas. Ga-68-PentixaFor PET demonstrates promising detection capabilities across various lymphomas, suggesting its potential as a superior imaging modality for low-grade lymphomas.

Participants needed: 15
Trial details
Phase: Phase 2Age: 20-100Biological sex: AllType: InterventionalSponsor: Koo Foundation Sun Yat-Sen Cancer CenterUpdated: Jun 14, 2024Locations: 1
Eligibility criteria

The pathological diagnosis is slow-growing lymphoma, such as: marginal-zone B-ce... [+5]

Pregnant woman [+6]