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NCT03116412Recruiting

A Randomized Trial to Assess the Role of Imaging During Follow Up After Radical Surgery of High Risk Melanoma

A Prospective Randomized Multicenter Trial to Assess the Role of Imaging During Follow Up After Radical Surgery of Stage IIb-c and III Cutaneous Malignant Melanoma

Source: ClinicalTrials.gov · Last updated 16 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

It is not known whether radiological assessments during follow up after surgery for high risk melanoma improve survival. Since radiological examinations are resource demanding, could inflict worry and cause irradiation exposure it is an important question to address. With the introduction of effective medical treatments for malignant melanoma patients, there is a tendency to introduce radiological assessments despite the lack of evidence.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
1300 (estimated)
First submitted
14 Mar 2017
Start date
8 Jun 2017
Primary completion date
31 Dec 2028
Lead sponsor
Uppsala University
Diseases
Melanoma
NCT number
NCT03116412

What you commit to

  • Study type: Interventional
  • Planned participants: 1300
  • From 8 Jun 2017 to the primary completion date, 31 Dec 2028
  • 20 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.

Prior treatment

  • Life-expectancy less than 2 years due to concurrent disease (e.g., cardiac disease, terminal multiple sclerosis, liver cirrhosis).

Other illness

  • Existing or previous malignancies within the past 5 years (except for in situ breast and cervical cancer, melanoma in situ and non-melanoma skin cancer).

Other

  • The patient is assessed as unfit to receive treatment in the case of recurrence.
  • Inability to provide informed consent or refusal to do so.
  • Inability to comply with the control or intense follow-up program.
  • Participation in other clinical trials interfering with the control-program.
  • Pregnancy or currently planned pregnancy.

Who the study is looking for

  • At least 18 years of age.
  • Radical surgery for Cutaneous Malignant Melanoma (CMM) stage IIb-c and III.
  • Sufficient renal function for i.v. contrast scannings.

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

Full criteria on ClinicalTrials.gov

Sites (20)

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

SiteCityCountrySite status
Södra Älvsborgs Sjukhus
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BoråsSwedenTerminated
Malarsjukhuset Eskilstuna
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EskilstunaSwedenRecruiting
Falu Lasarett
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FalunSwedenRecruiting
Gävle sjukhus
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GävleSwedenRecruiting
Department of Surgery, Sahlgrenska University Hospital
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GothenburgSwedenRecruiting
Helsingborgs lasarett
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HelsingborgSwedenRecruiting
Lanssjukhuset Ryhov
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JönköpingSwedenRecruiting
Länssjukhuset i Kalmar
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KalmarSwedenNot yet recruiting
Centralsjukhuset i Karlstad
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KarlstadSwedenRecruiting
Linkoping University Hospital
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LinköpingSwedenRecruiting
Skåne University Hospital
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MalmöSwedenRecruiting
Örebro University Hospital
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ÖrebroSwedenRecruiting
Skaraborgs sjukhus Skövde
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SkövdeSwedenTerminated
Karolinska University Hospital
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StockholmSwedenRecruiting
Länssjukhuset Sundsvall
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SundsvallSwedenRecruiting
Uddevalla sjukhus
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UddevallaSwedenTerminated
Umeå University Hospital
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UmeåSwedenTerminated
Akademiska sjukhuset
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UppsalaSwedenRecruiting
Västmanlands Sjukhus Västerås
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VästeråsSwedenRecruiting
Visby lasarett
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VisbySwedenRecruiting

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