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NCT01843881 · ClinicalTrials.gov registry record · Early Phase 1

The Contribution of Incretin Hormones to Post-prandial Glucose Metabolism After Roux-en-Y Gastric Bypass

A Early Phase 1 study of Type 2 Diabetes Mellitus, sponsored by Adrian Vella.

Completed
Registry status
Early Phase 1
Development phase
20
Enrollment target
1
Study location

NCT01843881 is a Early Phase 1 study of Type 2 Diabetes Mellitus that has completed, run by Adrian Vella. The registered enrollment target is 20 participants, below the 2,748-participant average among 122 other Type 2 Diabetes Mellitus trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01843881, a Early Phase 1 study of Type 2 Diabetes Mellitus, has completed, sponsored by Adrian Vella.

COMPLETED
Registry status
Early Phase 1
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

The study is being undertaken to understand how the Roux-en-Y Gastric Bypass procedure can affect insulin secretion after meals. The hypothesis of this study is the Disposition Index is decreased in subjects who had previously undergone Roux-en-Y Gastric Bypass by glucagon-like peptide-1 (GLP-1) receptor blockade.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Exendin 9, 39

Study Locations (1)

Minnesota

  • Mayo Clinic - Rochester

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2012-03
Est. Completion 2013-12
Phase Early Phase 1

Sponsor

Adrian Vella

9 total trials

What the Registry Record Tells You About NCT01843881

The ClinicalTrials.gov registry entry for NCT01843881 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,748-participant average among 122 other Type 2 Diabetes Mellitus trials with a reported enrollment target (99% lower). The listed sponsor is Adrian Vella, which has 9 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Type 2 Diabetes Mellitus appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT01843881 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT01843881 about?

NCT01843881 is a clinical study titled "The Contribution of Incretin Hormones to Post-prandial Glucose Metabolism After Roux-en-Y Gastric Bypass". The study is being undertaken to understand how the Roux-en-Y Gastric Bypass procedure can affect insulin secretion after meals. The hypothesis of this study is the Disposition Index is decreased in subjects who had previously undergone Roux-en-Y Gastric Bypass by glucagon-like peptide-1 (GLP-1) rec...

What is the current status of trial NCT01843881?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 20 participants. The study started on 2012-03. Estimated completion is 2013-12.

What conditions does trial NCT01843881 study?

This clinical trial studies the following conditions: Type 2 Diabetes Mellitus.

What interventions are being tested in trial NCT01843881?

The interventions under investigation include: Placebo (DRUG), Exendin 9, 39 (DRUG).

Who is sponsoring clinical trial NCT01843881?

This trial is sponsored by Adrian Vella, which has 9 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01843881 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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