An Investigational Scan (Dual Energy CT) in Detecting Gastrointestinal Carcinoid Tumors

NCT ID: NCT04993261

Last Updated: 2025-08-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

EARLY_PHASE1

Total Enrollment

71 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-23

Study Completion Date

2026-12-31

Brief Summary

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This trial studies the use of a special type of computed (CT) scan called dual energy CT in detecting gastrointestinal carcinoid tumors. CT is an imaging technique that uses x-rays and a computer to create images of areas inside the body. Dual energy computed tomography is a technique used during routine CT scans to help obtain and process the image after the scan is complete. Doctors want to learn if dual energy computed tomography can help improve the detection of carcinoid tumors during routine CT scans.

Detailed Description

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PRIMARY OBJECTIVES:

I. Evaluate prospectively the sensitivity and specificity of dual energy computed tomography (CT) in detecting primary gastrointestinal (GI) carcinoid.

OUTLINE:

Patients undergo one dual energy CT scan during scheduled CT scan.

Conditions

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Carcinoid Syndrome Carcinoid Tumor Digestive System Neuroendocrine Tumor G1 Metastatic Carcinoid Tumor

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Diagnostic (dual energy CT scan)

Patients undergo one dual energy CT scan during scheduled CT scan.

Group Type EXPERIMENTAL

Dual-Energy Computed Tomography

Intervention Type PROCEDURE

Undergo dual energy CT scan

Interventions

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Dual-Energy Computed Tomography

Undergo dual energy CT scan

Intervention Type PROCEDURE

Other Intervention Names

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DECT

Eligibility Criteria

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Inclusion Criteria

* Patients with: clinical features of carcinoid syndrome (or) increased serum and urinary markers suggestive of carcinoid (or) endoscopic biopsy proven carcinoid (or) metastases which are biopsy proven as carcinoid.
* Patient is scheduled to have a clinically indicated staging CT exam.
* Patients who have signed their informed consent form to undergo the study.

Exclusion Criteria

* Patients who have already had their primary GI carcinoid resected.
* Contraindication to intravenous contrast agents (e.g. allergy, renal failure, dialysis, pregnancy etc.).
* Pregnant patients.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ajaykumar Morani

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

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M D Anderson Cancer Center

Houston, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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NCI-2019-02477

Identifier Type: REGISTRY

Identifier Source: secondary_id

2014-0578

Identifier Type: OTHER

Identifier Source: secondary_id

2014-0578

Identifier Type: -

Identifier Source: org_study_id

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