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NCT06367010Completed

Clinical Efficacy of 125I Brachytherapy Combined With Anlotinib in Radioiodine Refractory Thyroid Carcinoma Patients

Clinical Efficacy and Safety Analysis of 125I Brachytherapy Combined With Anlotinib in Radioiodine Refractory Thyroid Carcinoma Patients

Source: ClinicalTrials.gov · Last updated 16 Apr 2024

Brief summary (registry, in English)

A retrospective analysis was conducted on patients with radioiodine-refractory thyroid carcinoma (RRTC) who underwent radioactive 125I seed implantation combined with anlotinib from January 2019 to October 2024 at Jiangxi Cancer Hospital. Data on tumor size changes before and after treatment, serological tests (including serum TG, TgAb, CTn, CEA, etc.), changes in patients' pain scores, and side effects were collected to evaluate the clinical efficacy and safety of this therapy.

Status (registry)
Completed
Study type
Observational
Enrollment
8 (actual)
First submitted
10 Apr 2024
Start date
1 Jan 2019
Primary completion date
1 Apr 2024
Lead sponsor
Jiangxi Provincial Cancer Hospital
NCT number
NCT06367010

What you commit to

  • Study type: Observational
  • Participants enrolled: 8
  • From 1 Jan 2019 to the primary completion date, 1 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • (v) Patients who are unable to cooperate with or tolerate particle implantation surgery;

Other illness

  • (iii) Patients with severe coagulation disorders;
  • (iv) Patients with severe cardiorespiratory impairment;

Other

  • (i) Patients who are positive for TgAb;
  • (ii) Patients with a TSH level of 0.1 mU/L or higher;
  • (vi) Patients with an expected survival period of less than 3 months.

Who the study is looking for

  • (i) Thyroid cancer confirmed through pathological examination;
  • (ii) Disease progression after conventional treatments, such as surgery, postoperative 131I, and external irradiation;
  • (iii) Multiple tumor foci, with at least one focus where the tumor's maximum diameter exceeds 3 cm.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Jiangxi Cancer Hospital
Coordinator of this site? Confirm its status
NanchangChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.