Personalized Quantum Sonotherapy in Regional Anesthesia

Anxiety Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03512587
• Other study ID #: 645
• Status: Completed
• Phase: N/A
• Start date: February 1, 2017
• Est. completion date: March 31, 2017

Study information

• Verified date: April 2018
• Source: CES University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: March 31, 2017
• Est. primary completion date: March 31, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

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.

Related Conditions & MeSH terms

• Anxiety
• Pain, Postoperative

Intervention

Procedure:
• Personalized 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.
• Placebo
Headphones will be place in patients without playing quantum sonotherapy

Locations

Country	Name	City	State
Colombia	Instituto Colombiano del Dolor	Medellin	Antioquia

Sponsors (1)

Lead Sponsor	Collaborator
CES University

Country where clinical trial is conducted

Colombia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain	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.	48 hours (From the moment before surgery when the sonotherapy is apply until 48 hours after surgery)
Primary	Anxiety	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.	48 hours (From the moment before surgery when the sonotherapy is apply until 48 hours after surgery)