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Determinants of Efficacy of EsophyX Treatment in Gastro-Esophageal Reflux Disease

Determinants of Efficacy of EsophyX Treatment in Gastro-Esophageal Reflux Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00498082
Enrollment
Unknown
Registered
2007-07-09
Start date
2007-09-30
Completion date
2008-09-30
Last updated
2007-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastroesophageal Reflux Disease

Brief summary

EsophyX is a promising endoscopic treatment for gastro-esophageal reflux disease. It is not known whether there are some pre- or per-operative anatomic or pathophysiological findings which may influence outcome. The aim of this trial is to study a series of parameters acquired during the pre-therapeutic work-up or during the procedure and their influence on the outcome of the procedure.

Interventions

None listed

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients being considered for EsophyX treatment of GERD

Countries

Belgium

Contacts

Primary ContactHubert Piessevaux, MD, PhD
piessevaux@gaen.ucl.ac.be+ 32 2 764 28 34

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026