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Trial Radar IA
Lo studio clinico NCT02707029 per Fisiologia normale, Dolore è in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui.
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Clinical and Scientific Assessment of Pain and Painful Disorders 10.000

In arruolamento
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT02707029 è uno studio osservazionale per Fisiologia normale, Dolore, attualmente in arruolamento. Avviato il 22 luglio 2016, prevede di arruolare 10.000 partecipanti. Sotto la guida di National Center for Complementary and Integrative Health (NCCIH), dovrebbe concludersi entro il 9 febbraio 2027. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 24 febbraio 2026.
Sommario breve
Background:

Researchers want to better understand pain by studying people with and without different kinds of pain. To do this, researchers will expose people to pleasant and unpleasant sensations. They will ask them questions about their pain. Researchers also want to see if these people are eligible for other research studies at the National Center for Complementary and Integrative Health.

Objectives:

To study t...

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Descrizione dettagliata
Objective:

The purpose of this study is to allow for the deep, broad, and targeted phenotyping of persons with or without pain disorders. This protocol will enable NCCIH investigators to describe the clinical aspects of pain disorders, collect scientific measurements for the purpose of making deep phenotypic descriptions, and use the collected data to perform descriptive analyses of pain disorders. The study will al...

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Titolo ufficiale

Clinical and Scientific Assessment of Pain and Painful Disorders

Patologie
Fisiologia normaleDolore
Pubblicazioni
Articoli scientifici e documenti di ricerca pubblicati su questo studio clinico:
Altri ID dello studio
  • 160077
  • 16-AT-0077
Numero NCT
Data di inizio (effettiva)
2016-07-22
Ultimo aggiornamento pubblicato
2026-02-24
Data di completamento (stimata)
2027-02-09
Arruolamento (previsto)
10.000
Tipo di studio
Osservazionale
Stato
In arruolamento
Parole chiave
Screening Protocol
Pain
Phenotypes
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
Persons, with or without pain disorders
Adults and adolescents with or without pain disorders.
N.D.
Esito primario
Misure di esitoDescrizione della misuraArco temporale
To enable for the deep, broad, and targeted phenotyping of individuals, in particular those with rare and unusual pain disorders.
Data are to be collected via medical history, physical examinations, questionnaires, laboratory samples and MRI imaging.
36 months
Esito secondario
Misure di esitoDescrizione della misuraArco temporale
To facilitate obtaining information relevant to determining potential eligibility in IRB-approved NIH protocols, in particular those of the Clinical Investigations Branch of NCCIH.
Data are to be collected via medical history, physical examinations, questionnaires, laboratory samples and MRI imaging.
36 months
Assistente alla partecipazione
Criteri di eleggibilità

Età idonea
Bambino, Adulto, Adulto anziano
Età minima
12 Years
Sessi idonei
Tutti
Accetta volontari sani
  • Are >= 12 years of age

  • Have difficulties with communication that make subjective pain assessment impossible or unreliable.
  • Have acute medical or psychiatric health issues that create additional and substantial adverse risks related to study procedures. Medical examples are the acute complications of medical disease, such as asymptomatic hypertensive urgency, diabetic ketoacidosis, symptomatic hyperthyroidism, and unstable angina. Psychiatric examples are the acute complications of psychiatric disease, such as acute mania, paranoid delusions, or having acute panic attacks.
  • Are participating in other ongoing research protocols such that phenotypic measurements would interfere with the conduct of an ongoing protocols or the receipt of a research treatment would influence the phenotypic measurements.
  • Employees or staff that work at NCCIH.
  • Pregnant women
National Center for Complementary and Integrative Health (NCCIH) logoNational Center for Complementary and Integrative Health (NCCIH)
Contatti principali dello studio
Contatto: Keyonna L Berry, (301) 594-1782, [email protected]
Contatto: Miroslav Backonja, M.D., (301) 402-5679, [email protected]
1 Centri dello studio in 1 paesi

Maryland

National Institutes of Health Clinical Center, Bethesda, Maryland, 20892, United States
For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR), Contatto, 800-411-1222, [email protected]
In arruolamento