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Completed Not applicable Interventional

Study of Weight Loss Using Gastric Stimulation in Obese Patients

ClinicalTrials.gov ID: NCT00200083

Public ClinicalTrials.gov record NCT00200083. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 6, 2026, 9:48 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SHAPE: Screened Health Assessment & Pacer Evaluation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to test the effect of an implanted device that stimulates the stomach to help obese patients lose weight.

Study identification

NCT ID
NCT00200083
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
MedtronicNeuro
Industry
Enrollment
190 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2004 (Type not available)
Primary completion
Sep 2005 (Actual)
Completion
Jan 2008 (Actual)
Last update posted
Mar 27, 2015

2004 – 2008

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Contact Medtronic for specific site information Washington D.C. District of Columbia 20037 —
Contact Medtronic for specfici site information Gainsville Florida 32611 —
Contact Medtronic for specific site information Chicago Illinois 60611 —
Contact Medtronic for specific site information Boston Massachusetts 02111 —
Contact Medtronic for specific site information Minneapolis Minnesota 55416 —
Contact Medtronic for specific site information St Louis Missouri 60611 —
Contact Medtronic for specific site information New York New York 10032 —
Contact Medtronic for specific site information Philadelphia Pennsylvania 19140 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00200083, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 27, 2015 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00200083 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →