Clinical trial · Observational
Endoscopic Submucosal Dissection for Early GI Neoplasia in the United Kingdom
Endoscopic Submucosal Dissection in the Treatment of Early Gastrointestinal Neoplasia: A UK Cohort Study to Assess Effectiveness and Safety
NCT03039309CI-TRIAL-00116235ESDUKrecruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 18, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260918-000001
Summary
Brief summary (as posted)
Multicentre cohort study on the use of endoscopic submucosal dissection for the treatment of early gastrointestinal neoplasia.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Endoscopic Submucosal Dissection | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Endoscopic Submucosal Dissection | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Curative resection rate
- timeFrame
- 2 years
- description
- % of successful resections free of disease at follow up endoscopy by the end of the follow up period (2 years)
Secondary outcomes (3)
- measure
- En bloc resection rate
- timeFrame
- At the time of procedure
- description
- % of en bloc resections obtained at the time of initial endoscopic submucosal dissection
- measure
- Complication rates
- timeFrame
- 28 days post procedure
- description
- % of complications noted within 28 days following endoscopic submucosal dissection
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Male or Female, aged 18 years or above undergoing endoscopic submucosal dissection * Participant is able to give informed consent for participation in the study Exclusion Criteria: * Patients under the age of 18 * Patients unable to give informed consent
References
Publications (0)
Data not yet available
No reference posted for this study.