No registrations found.
ID
Source
Brief title
Health condition
Barrett's Esophagus, Barrett's neoplasia, endoscopic treatment, endoscopic ablation, RFA, cryoablation, endoscopic resection, EMR, ESD
Sponsors and support
Intervention
Outcome measures
Primary outcome
Cumulative pain through 14 days, defined as the area under the curve for a pain versus time (14 days) plot
Secondary outcome
Cumulative dysphagia, cumulative use of analgesics, peak pain score, duration of pain
Background summary
This is a continuous, prospective registration that includes all patients undergoing endoscopic therapy for Barrett's esophagus as part of regular clinical care. The addition of this study, includes a 14 days digital diary that will be sent to all patients to assess pain, dysphagia and use of pain killers. The need for IRB approval was waived by the IRB of the MEC-U.
Study design
Treatment endoscopy; 14 days digital diary; follow-up endoscopy
Intervention
Patients receive a 14 days digital diary to assess retrosternal pain (range 0-10), dysphagia (range 0-4) and use of analgesics (yes/no, type).
Inclusion criteria
All patients (all age, both sexes) undergoing endoscopic therapy for Barrett's esophagus, that consent to complete a 14-days digital diary post-procedure
Exclusion criteria
No access to e-mail
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL6672 |
| NTR-old | NTR6906 |
| Other | W15.100 : 1001 |