Clinical trial · Observational
Study to Evaluate the Use of Resources and the Costs Associated With Carcinoid Syndrome (CS) in Patients With NETs in Spain
Study to Evaluate the Use of Resources and the Costs Associated With Controlled or Uncontrolled Carcinoid Syndrome in Patients With Neuroendocrine Tumours (NETs) in Spain
NCT03220087CI-TRIAL-00036248RECOSYcompletedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The objective of this study is to describe the use of resources and the costs associated with controlled or uncontrolled CS in patients with NETs in Spain.
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 |
|---|---|---|---|
| Neuroendocrine Tumors | Neuroendocrine Tumor | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Data collection | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Group A - Uncontrolled CS
- description
- Patients who have had at least one episode of uncontrolled CS, according to medical criteria, since the start of their treatment for NET.
- interventionNames
- Other: Data collection
- label
- Group B - Controlled CS
- description
- Patients who have not had any episode of uncontrolled CS, according to medical criteria, in the last 12 months.
- interventionNames
- Other: Data collection
Primary outcomes (1)
- measure
- Use of resources and costs in patients with controlled or uncontrolled CS
- timeFrame
- Day 1 (Group A retrospective data collection - 3 months before and up to 6/12 months after the last uncontrolled carcinoid episode. Group B retrospective data collection - up to 6/12 months before the date of enrolment)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patient 18 years of age or older. * Patient with a diagnosis of NET (G1 or G2) treated with Somatostatin Analogues (SSAs) to manage their symptoms. 1. Group A: patient who has had at least one episode of uncontrolled CS, according to medical criteria, since the start of treatment. 2. Group B: patient who has not had any episode of uncontrolled CS, according to medical criteria, in the last 12 months. * Patient able to read and understand the study questionnaires. * Patient who has given written informed consent to participate in the study. Exclusion Criteria: * Patient participating in another clinical study when invited to participate in this study. * Patient with another severe malignant disease. * Patient who cannot meet the requirements established in the protocol (non-compliant or unfit to fill in the questionnaires). * Patient with symptoms or diseases that could be confused with CS or render CS more difficult to evaluate: right cardiomyopathy or diarrhoea of any aetiology other than NET.
References
Publications (0)
Data not yet available
No reference posted for this study.