18F-FDG and 68Ga-FAPI PET/CT in Crohn's Disease
Primary Purpose
Crohn Disease
Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
18F-FDG and 68Ga-FAPI PET/CT
Sponsored by
About this trial
This is an interventional diagnostic trial for Crohn Disease
Eligibility Criteria
Inclusion Criteria:
- Written informed consent signed
- Crohn's disease patients with proofs of intestine stricture by other modalities, e.g. MRI, CT, ultrasound, and/or endoscopy.
Exclusion Criteria:
- Known hypersensitivity to any of the excipients of 18F-FDG and 68Ga-FAPI.
- If the patients are on metformin, discontinuation of 48 hours is required before 18F-FDG injection to minimize the bowel uptake.
- Pregnant or breast-feeding women.
- Any mental condition rendering the patient unable to understand the nature, scope, and possible consequences of the study, and/or evidence of an uncooperative attitude.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Crohn's disease: patients with intestinal stricture
Arm Description
Patients with intestinal strictures confirmed by other modalities, e.g. CT, MR, ultrasound, and endoscopy, will be recruited in the study.
Outcomes
Primary Outcome Measures
SUVmax of stenotic intestine
The SUVmax of stenotic intestine will be determined on 18F-FDG and 68Ga-FAPI PET scan to reflect the highest extent of inflammation and fibrosis, respectively.
MV of stenotic intestine
The MV of stenotic intestine will be determined on 18F-FDG and 68Ga-FAPI PET scan to reflect the involved area of inflammation and fibrosis, respectively.
TMI of stenotic intestine
The TMI of stenotic intestine will be determined on 18F-FDG and 68Ga-FAPI PET scan to reflect the overall extent of inflammation and fibrosis, respectively.
Secondary Outcome Measures
Histological findings
In patients with surgical resection of stenotic intestine, the extent of inflammation and fibrosis will be determined.
Full Information
NCT ID
NCT04502303
First Posted
August 4, 2020
Last Updated
August 5, 2020
Sponsor
Peking Union Medical College Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04502303
Brief Title
18F-FDG and 68Ga-FAPI PET/CT in Crohn's Disease
Official Title
A Prospective Study to Evaluate the Inflammation and Fibrosis of Intestinal Stricture in Patients With Crohn's Disease by 18F-FDG and 68Ga-FAPI PET/CT
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 2020 (Anticipated)
Primary Completion Date
September 2021 (Anticipated)
Study Completion Date
September 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Intestinal stricture is a complication of Crohn's disease (CD), which is thought to be the result of chronic transmural inflammation combined with a dysregulated wound-healing process. While inflammatory strictures may respond to anti-inflammatory treatment, fibrotic strictures are usually anti-inflammation resistant, requiring further endoscopic balloon dilation or surgical intervention. Therefore, to determinate the inflammatory or fibrotic nature of intestinal stricture is a key step in the treatment of CD. 18F-FDG is a radiotracer reflecting the glucose metabolism of disease and is usually accumulated in inflammatory disease. 68Ga-FAPI is a novel radiotracer that specifically targets fibroblast activation protein (FAP). FAP is a membrane glycoprotein expressed on activated fibroblasts, which are key cells in the process of fibrotic intestinal stricture of CD. In this study, we hypothesis that the inflammatory or fibrotic nature of intestinal stricture can be non-invasively evaluated by 18F-FDG and 68Ga-FAPI PET/CT in patients with CD.
Detailed Description
Patients with intestinal stricture will undergo 18F-FDG and 68Ga-FAPI PET/CT on two consectutive days. The accumulation of 18F-FDG and 68Ga-FAPI at the site of stricture will be determined by standard uptake value (SUV), molecular volume (MV), and total molecular index (TMI). In patients with a planned surgical resection of one or more stricture (s), the image results will be compared with histological findings.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Patients with intestinal stricture will undergo 18F-FDG and 68Ga-FAPI PET/CT on two consecutive days.
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Crohn's disease: patients with intestinal stricture
Arm Type
Experimental
Arm Description
Patients with intestinal strictures confirmed by other modalities, e.g. CT, MR, ultrasound, and endoscopy, will be recruited in the study.
Intervention Type
Diagnostic Test
Intervention Name(s)
18F-FDG and 68Ga-FAPI PET/CT
Intervention Description
Participants will undergo 18F-FDG (0.12-0.15mCi/kg) and 68Ga-FAPI (3-6mCi) PET/CT on two consecutive days. At least 6 hours of fast is required for 18F-FDG PET scan, while no dietary control is necessary for 68Ga-FAPI PET scan. If the patients are on metformin, discontinuation of 48 hours is required before 18F-FDG injection to minimize the bowel uptake. If the patient is planned for surgical resection of one or more stricture (s), the scans have to be completed within a maximum period of 30 days before the surgery.
Primary Outcome Measure Information:
Title
SUVmax of stenotic intestine
Description
The SUVmax of stenotic intestine will be determined on 18F-FDG and 68Ga-FAPI PET scan to reflect the highest extent of inflammation and fibrosis, respectively.
Time Frame
Day 30 after PET scan
Title
MV of stenotic intestine
Description
The MV of stenotic intestine will be determined on 18F-FDG and 68Ga-FAPI PET scan to reflect the involved area of inflammation and fibrosis, respectively.
Time Frame
Day 30 after PET scan
Title
TMI of stenotic intestine
Description
The TMI of stenotic intestine will be determined on 18F-FDG and 68Ga-FAPI PET scan to reflect the overall extent of inflammation and fibrosis, respectively.
Time Frame
Day 30 after PET scan
Secondary Outcome Measure Information:
Title
Histological findings
Description
In patients with surgical resection of stenotic intestine, the extent of inflammation and fibrosis will be determined.
Time Frame
Day 90 after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Written informed consent signed
Crohn's disease patients with proofs of intestine stricture by other modalities, e.g. MRI, CT, ultrasound, and/or endoscopy.
Exclusion Criteria:
Known hypersensitivity to any of the excipients of 18F-FDG and 68Ga-FAPI.
If the patients are on metformin, discontinuation of 48 hours is required before 18F-FDG injection to minimize the bowel uptake.
Pregnant or breast-feeding women.
Any mental condition rendering the patient unable to understand the nature, scope, and possible consequences of the study, and/or evidence of an uncooperative attitude.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wenjia Zhu, MD
Phone
+86 18614080164
Email
zhuwenjia_pumc@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Li Huo, MD
Phone
+86 13910801986
Email
zhuwenjia_pumc@163.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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18F-FDG and 68Ga-FAPI PET/CT in Crohn's Disease
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