Evaluation of Heart Rate Variability in Third Lower Molars Surgeries
NCT ID: NCT01910337
Last Updated: 2013-07-29
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.
COMPLETED
33 participants
OBSERVATIONAL
2011-06-30
2012-03-31
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.
Plethysmographic Waveform for Monitoring the Quality of Cardiopulmonary Resuscitation
NCT01987245
Temperature and Analgesia Monitoring During Cardial Parmonary Bypass
NCT03358680
Heart Rate Variability in Pneumothorax
NCT03537417
The Value of Continuous Noninvasive Hemoglobin Monitoring Using Masimo Radical -7 Pulse CO-Oximeter in Intraoperative Blood Transfusion Practice During Obstetric Procedures
NCT03408938
The Effect of a Real-time Audiovisual Feedback System on CPR Quality
NCT03902873
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.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Screening
this first day, the patient will be evaluated with polar and blood pressure monitor. These data will be the basal one.
Use the Polar Cardiac rate meter
Intervation
One week later the screening, the patient underwent to the surgery to remove his lower third molar. In this day, will be analyzed 4 points: basal, after the anesthesia, after the avulsion and 20 minutes after the surgery.
Use the Polar Cardiac rate meter
Post operative
One week later the surgery, the patients will be evaluated again.
Use the Polar Cardiac rate meter
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Use the Polar Cardiac rate meter
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Need to remove one of Lower Third Molar.
Exclusion Criteria
* pregnant
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Sao Paulo
OTHER
Renata Martins da Silva Prado
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Renata Martins da Silva Prado
2926480
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculdade de Odontologia da Universidade de são Paulo
São Paulo, São Paulo, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FR335167
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.