Feasibility and Effects of Noninvasive Brain Stimulation on Pain Perception in People With Fibromyalgia
A legfontosabb adatok
- Hol
- Pittsburgh (Egyesült Államok)Mind a 2 helyszín megnézése
Neked szólhat?
Magadról válaszolj. Ez nem döntés: hogy részt vehetsz-e, azt csak a vizsgálat csapata mondhatja meg.
- 18 és 65 év között vagy?
Forrás: NCT07644221: ki vehet részt
Helyszínek itt: Egyesült Államok
- Carnegie Mellon UniversityPittsburgh, Egyesült ÁllamokContact: Pulkit Grover, PhDToborzás még nem indult
- UPMC Pain ManagementPittsburgh, Egyesült ÁllamokContact: Benedict J Alter, MD, PhDRésztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Pulkit Grover
- Azonosító
- NCT07644221
- A regiszteradat frissítve
- 2026. október 21.
- Eredeti leírás
The goal of this interventional study is to learn whether noninvasive brain stimulation (NIBS) will have an effect on pain perception in people with fibromyalgia. The main questions it aims to answer are:A teljes eredeti leírásKevesebb
Transcranial Electrical Stimulation for Noninvasive Study of Pain Circuits in Patients With Chronic Pain
The goal of this interventional study is to learn whether noninvasive brain stimulation (NIBS) will have an effect on pain perception in people with fibromyalgia. The main questions it aims to answer are:
Do repeated sessions of NIBS lead to a reduction in perceived pain? Do repeated sessions of NIBS lead to an improvement in quality of life?
Researchers will compare different brain targets to see if effects are different between them.
Participants will receive repeated daily sessions of NIBS over 4 weeks with application of pressure pain algometry, and complete various questionnaires.
Bevonási feltételek: Formal diagnosis of fibromyalgia made by a practicing physician; Pain resistant to common analgesics and medications for chronic pain; Existing pain for more than 3 months with an average of at least 4 on a 0 to 10 Numerical Rating Scale (NRS); Females of child bearing potential must be at least one of the following totally abstinent from heterosexual intercourse since the last menses before start of study, or agree to concurrent use of at least two methods of birth control throughout study participation.
Kizáró feltételek: Subject must not have a history of brain surgery or uncontrolled neurological conditions, such as seizure, fainting spells, transient ischemic attack; Subject must not have lifetime history of severe, uncontrolled mood disorders (anxiety, depression, bipolar), psychotic disorders, other neural disorders, or heart disease; Subject must not have heart diseases, including known arrhythmia, or severe liver or severe gastrointestinal disease or chronic severe infectious disease (e.g. HIV/AIDS); If the subject is non-ambulatory; If the subject is female of child-bearing potential, subject must not be pregnant; Subject must not have any implanted electronic or metallic devices.