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Personalized Quantum Sonotherapy in Regional Anesthesia

Personalized Quantum Sonotherapy in Regional Anesthesia Peripheral Nerve Block: Randomized and Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03512587
Enrollment
80
Registered
2018-05-01
Start date
2017-02-01
Completion date
2017-03-31
Last updated
2018-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Pain, Postoperative

Keywords

Personalized quantum sonotherapy, Regional anesthesia, Peripheral nerve block

Brief summary

The objetive of the study is to evaluate the effect of personalized quantum sonotherapy on the level of anxiety and pain in outpatients schedule for orthopedic surgery under regional anesthesia in a second level center. The investigators believed that personalized quantum sonotherapy could reduce the levels of anxiety and pain before and after surgery evaluated through hemodynamic variables and scales for pain (analogous visual scale) and anxiety (STAI Spielberger anxious state questionnaire).

Interventions

PROCEDUREPersonalized quantum sonotherapy

Quantum sonotherapy is an alternative non-pharmacological treatment that effects a molecular reorganization that occurs after the sound stimulus. The audible words and their waves have the ability to generate vibrations and stimulate the psycho-neuro-endocrine chain, independent of the semantic meaning of the words. It is an alternative therapy that uses non-musical sound waves.

PROCEDUREPlacebo

Headphones will be place in patients without playing quantum sonotherapy

Sponsors

CES University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients scheduled for elective orthopedic ambulatory surgery under regional anesthesia * Age between 18 and 60 years. * Patients with anesthetic risk ASA 1 and 2. * Patients without contraindications for the administration of opioids and benzodiazepines. * Patients living in the metropolitan area who have a telephone line and can be contacted by telephone within the first 48 hours through calls at 24 and 48 hours after surgery, made by the researchers at the number previously reported by the patient. * Patients with an adequate level of understanding, who are able to communicate by telephone and understand a numerical scale. * Patients who agree to participate in the work.

Exclusion criteria

* Patients with auditory and cognitive problems. * Patients requiring general anesthesia at some time during the intraoperative period. * Patients with morbid obesity. * Patients consuming anxiolytics in the last month. * Patients whose start of surgery is after 45 minutes of the blockade.

Design outcomes

Primary

MeasureTime frameDescription
Pain48 hours (From the moment before surgery when the sonotherapy is apply until 48 hours after surgery)To assess the effect of personalized quantum sonotherapy on the level of pain of patients taken to orthopedic surgery under regional anesthesia through pain score visual analoge score (VAS). VAS ranges from 0 to 10 being 0 no pain an 10 the worst pain ever felted. It would be measured before and after placing de sonotherapy, 24 and 48 hour after surgery.
Anxiety48 hours (From the moment before surgery when the sonotherapy is apply until 48 hours after surgery)To assess the effect of personalized quantum sonotherapy on the level of anxiety of patients taken to orthopedic surgery under regional anesthesia through anxiety score Questionnaire of anxious state STAI (Spielberger). STAI is a score to meausre anxiety, it has 20 questions each one with a possible value from 0 to 3 points. Total score is evaluated adding each score for each question, and it goes from 0 to 60 points, being 60 de higest score for anxiety. It would be measured before and after placing de sonotherapy, 24 and 48 hour after surgery.

Countries

Colombia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026