Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
100 participants
OBSERVATIONAL
2010-07-31
2012-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Peripheral Arterial Tonometry (PAT) Evaluation of Sleep in Fibromyalgia
NCT01151163
Investigation of the Relationship Between Sensory Processing and Kinesychophobia in Fibromyalgia Patients
NCT03746379
HRV Biofeedback in Fibromyalgia
NCT00222274
Heart Rate Variability in Fibromyalgia - Effects of Strengthening Exercises
NCT02004405
Pain Processing in Inflammatory and Non-Inflammatory Chronic Pain Syndromes
NCT05277025
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients diagnosed with Fibromyalgia
Evaluation of autonomic parameters
Physical examination, ECG, Loop recorder, Heart rate variability evaluation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Evaluation of autonomic parameters
Physical examination, ECG, Loop recorder, Heart rate variability evaluation
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Tenderness in 11 of 18 points
Exclusion Criteria
* Known tachyarrhythmia
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Tel-Aviv Sourasky Medical Center
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Tel Aviv Sourasky medical center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Tel Aviv Sourasky medical center
Tel Aviv, , Israel
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Jacob N Ablin, MD
Role: CONTACT
Michael Barkagan, MD
Role: CONTACT
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TASMC-10-JA-0678-09-CTIL
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.