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NCT03605771Active, not recruiting

Descriptive Observational Study on the Characteristics of Advanced and Metastatic Melanoma in Spain

Source: ClinicalTrials.gov · Last updated 17 Sept 2026

Brief summary (registry, in English)

This is an observational, multicentre epidemiological study with a longitudinal cohort in which information will be retrieved from medical records of patients with advanced metastatic or unresectable melanoma at first diagnosis.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
400 (estimated)
First submitted
20 Jul 2018
Start date
7 Aug 2018
Primary completion date
31 Dec 2027
Lead sponsor
Grupo Español Multidisciplinar de Melanoma
Diseases
Melanoma
NCT number
NCT03605771

What you commit to

  • Study type: Observational
  • Planned participants: 400
  • From 7 Aug 2018 to the primary completion date, 31 Dec 2027
  • 39 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Any patient not complying with inclusion criteria.

Who the study is looking for

  • Patients of legal age with stage III, metastatic, or unresectable melanoma at first diagnosis after January 8, 2018. First diagnosis is understood as: a. Disease onset as metastatic or unresectable disease; b. First metastatic or unresectable relapse in the pre-established dates (after January 8, 2018) in a patient with previous localised melanoma and completely resected on dates before the pre-inclusion period.
  • Signing the Informed Consent Form (ICF).
  • A patient may have received the first or subsequent treatments for metastatic or unresectable disease in a hospital other than the centre where the ICF was signed, as long as the patient meets the inclusion criteria 1.
  • A patient can only sign one ICF (cannot sign an ICF in two different centres).
  • If a patient signs the ICF in a centre during the first-line therapy and then goes to another centre with consideration for the following lines: If the centre is associated with the GEM-1801 study, researchers will do their best to update the following lines and the patient status, introducing the new information in the centre where the ICF was initially signed. This information will be provided by the patient before contacting the principal investigator and always with prior consent of the patient, who will have previously provided the consent to contact by telephone for this purpose. If this second (or subsequent) centre is not associated with the GEM- 1801 study, this will be considered loss of follow-up, unless the patient returns to the GEM-1801 start centre, wherein the reporting physicians will do their best to update the information from other centres, always with prior patient consent, who will have previously signed the ICF; c) A patient card with the assigned code will be delivered.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (39)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Virgen de Los Lirios
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AlcoySpainUnknown status
Hospital La Ribera
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AlziraSpainUnknown status
Instituto Catalán de Oncología Badalona
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BadalonaSpainUnknown status
Hospital Universitari Vall d'Hebron
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BarcelonaSpainUnknown status
Hospital de la Santa Creu y Sant Pau
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BarcelonaSpainUnknown status
Hospital Universitario Quiron Dexeus
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BarcelonaSpainUnknown status
Hospital Universitario De Burgos
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BurgosSpainUnknown status
Hospital Universitario San Pedro Alcántara
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CáceresSpainUnknown status
Hospital General de Ciudad Real
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Ciudad RealSpainUnknown status
Onkologikoa
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Donostia / San SebastianSpainUnknown status
Hospital Clínico Universitario Virgen de la Arrixaca
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El PalmarSpainUnknown status
Hospital Universitario Virgen de las Nieves
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GranadaSpainUnknown status
Onconogranada
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GranadaSpainUnknown status
Hospital San Pedro
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LogroñoSpainUnknown status
Hospital Lucus Augusti
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LugoSpainUnknown status
Hospital General Universitario Gregorio Marañón
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MadridSpainUnknown status
Hospital Universitario La Paz
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MadridSpainUnknown status
Hospital Universitario Ramón y Cajal
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MadridSpainUnknown status
Hospital Clínico San Carlos
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MadridSpainUnknown status
Hospital Universitario la Princesa
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MadridSpainUnknown status
Hospital Universitario Puerta de Hierro - Majadahonda
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MajadahondaSpainUnknown status
Hospital Universitario Regional de Málaga
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MálagaSpainUnknown status
Hospital Costa del Sol
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MarbellaSpainUnknown status
Hospital Universitario Son Llatzer
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Palma de MallorcaSpainUnknown status
Complejo Hospitalario de Navarra
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PamplonaSpainUnknown status
Clínica Universidad de navarra
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PamplonaSpainUnknown status
Complejo Hospitalario de Pontevedra
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PontevedraSpainUnknown status
Parc Taulí
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SabadellSpainUnknown status
Complejo Asistencial Universitario de Salamanca
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SalamancaSpainUnknown status
Hospital Universitario Marqués de Valdecilla
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SantanderSpainUnknown status
Hospital Universitario de Valme
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SevilleSpainUnknown status
Hospital Virgen de la Salud
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ToledoSpainUnknown status
Hospital General Universitario de Valencia
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ValenciaSpainUnknown status
Instituto Valenciano de Oncologia
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ValenciaSpainUnknown status
Hospital Universitario Rio Hortega
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ValladolidSpainUnknown status
Hospital Clínico Universitario de Valladolid
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ValladolidSpainUnknown status
Hospital Universitario Araba Txagorritxu Victoria
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Vitoria-GasteizSpainUnknown status
Hospital Universitario Miguel Servet
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ZaragozaSpainUnknown status
Hospital Clinico Universitario Lozano Blesa
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ZaragozaSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.