Actively Recruiting

Phase 1
Phase 2
Age: 10Years - 80Years
All Genders
ID07350707

CXCR4-Targeted PET Imaging for the Differential Diagnosis of ACTH-Dependent and ACTH-Independent Cushing's Syndrome: A Prospective Observational Study

Led by Peking Union Medical College Hospital · Updated on 2026-01-20

160

Participants Needed

1

Research Sites

49 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the use of CXCR4-targeted PET/CT imaging with 68Ga-Pentixafor to improve the diagnosis of Cushing's syndrome, focusing on differentiating between ACTH-dependent and ACTH-independent types. This prospective observational study aims to assess how well this imaging method works compared to conventional techniques and, when available, 68Ga-DOTATATE PET/CT. The study is conducted by the Nuclear Medicine team at Peking Union Medical College Hospital, leveraging their expertise in neuroendocrine tumor imaging.

CONDITIONS

Brief Title

Diagnostic Value of CXCR4-targeted PET/CT in ACTH-dependent and Independent Cushing's Syndrome

Who Can Participate

Age: 10Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical suspicion or confirmed diagnosis of Cushing's syndrome based on symptoms or abnormal cortisol tests
  • Able and willing to undergo PET/CT imaging with 68Ga-Pentixafor and, when applicable, 68Ga-DOTATATE
  • Willing to provide informed consent for study participation
Not Eligible

You will not qualify if you...

  • Prior use of therapeutic or investigational radiopharmaceuticals within 5 physical half-lives before imaging
  • Pregnancy or breastfeeding
  • History of allergic reaction to gallium-based tracers or related compounds
  • Clinically unstable condition or severe organ dysfunction interfering with imaging or participation
  • Inability to complete required PET/CT imaging due to clinical or logistical reasons

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 day

Participants undergo PET/CT imaging with 68Ga-Pentixafor to evaluate CXCR4 expression patterns for differential diagnosis of Cushing's syndrome. Additional 68Ga-DOTATATE PET/CT scans may be performed if ectopic ACTH syndrome is suspected.

1 to 2 visits depending on imaging required

Long-term Monitoring

Duration - Approximately 12 months

Participants are monitored over approximately 12 months to evaluate diagnostic outcomes and disease progression.

Follow-up visits as determined by clinical need

Trial Site Locations

Total: 1 location

1

Peking Union Medical College Hospital

Beijing, Beijing Municipality, China, 100730

Actively Recruiting

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Research Team

Z

Zhaohui Zhu, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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