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ACTIVE NOT RECRUITING

Outcomes After Medical and Surgical Treatment of Gastroesophageal Reflux Disease

NCT00260572 · View on ClinicalTrials.gov ↗

Study Summary

The aims of this study are to create a prospective data base to evaluate the long term outcomes of medical and surgical treatment of gastroesophageal reflux disease (GERD); to measure standard outcomes as well as patient derived outcomes such as general and disease specific quality of life (QOL) issues and patient satisfaction; to refine the parameters that may identify patients who will benefit from surgery for GERD; and to identify possible determinants of failure of both medical and surgical treatments of reflux.

Interventions

  • BEHAVIORAL Questionnaires to evaluate QOL
  • BEHAVIORAL Questionnaires to evaluate heartburn and quality of life
  • BEHAVIORAL Questionnaire to evaluate satisfaction with treatment
  • BEHAVIORAL Questionnaire to evaluate presence or absence of pain

Study Locations (1)

Pennsylvania

  • UPMC Department of Cardiothoracic Surgery — Pittsburgh

Trial Details

FieldValue
Enrollment Target 2,500 participants
Start Date 1999-04
Est. Completion 2050-12

Sponsor

University of Pittsburgh

1,082 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00260572

The ClinicalTrials.gov registry entry for NCT00260572 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pittsburgh, which has 1,082 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Gastroesophageal Reflux Disease appearing as the primary indexed condition, and to 4 interventions — of which Questionnaires to evaluate QOL is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00260572 reports 1 study location spanning 1 distinct geographic area — top geographies include Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00260572 about?

NCT00260572 is a clinical study titled "Outcomes After Medical and Surgical Treatment of Gastroesophageal Reflux Disease". The aims of this study are to create a prospective data base to evaluate the long term outcomes of medical and surgical treatment of gastroesophageal reflux disease (GERD); to measure standard outcomes as well as patient derived outcomes such as general and disease specific quality of life (QOL) iss...

What is the current status of trial NCT00260572?

This trial is currently active not recruiting. The enrollment target is 2,500 participants. The study started on 1999-04. Estimated completion is 2050-12.

What conditions does trial NCT00260572 study?

This clinical trial studies the following conditions: Gastroesophageal Reflux Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00260572?

The interventions under investigation include: Questionnaires to evaluate QOL (BEHAVIORAL), Questionnaires to evaluate heartburn and quality of life (BEHAVIORAL), Questionnaire to evaluate satisfaction with treatment (BEHAVIORAL), Questionnaire to evaluate presence or absence of pain (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00260572?

This trial is sponsored by University of Pittsburgh, which has 1,082 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00260572 being conducted?

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

Related

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