Skip to main content
OpenTrials
Completed

NCT Number: NCT03925571

Musicotherapy in Reducing Peroperative Anxiety and Post-surgical Pain in Dental Care

The main purpose of MUSANX study is to highlight analgesic effectiveness of musicotherapy in post-surgical periodontal and implant; and to measure its per-operative anxiolytic effectiveness

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nantes University Hospital

Nantes, 44093, France

About this study

This study will be on music use as musicotherapy "receptive " or " passive ", using hearing aid for listening in order to relax and reduce the anxiety and pain state of the patient. This care will be focused on the acute stress and pain during the dental care.

Another major secondary purpose will consist to explore the anxiolytic effect of the musicotherapy on diverse stress markers such as heart rate, respiratory rate, salivary cortisol ratio and electro-dermal intensity (RED).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Majors aged between 18 and 55 years, with an appropriate hearing and able to use Music-Care© (selection of the playlist via internet access),
  • Needing treatment in odontology - periodontal surgery (coronary elongation or sanitation surgery or muco-gingival surgery) or implantary surgery (placement of an unit implant or two implant in the same localization),
  • Oral and dated consent,
  • Agreeing to be contacted via phone at J+1 and to fill follow-up study documents,
  • Profiting of social security or CMU.

Exclusion criteria

  • Patients with a long-term taking of anxiolytic or analgesic,
  • Regular consumer of soft drug (cannabis) or hard drug (opioid),
  • Patient with medical history of psychiatry (mental harm), hearing problem, cognitive and behavioural impairment (claustrophobia), sensory disabilities,
  • Patient with problems of hemostasis,
  • Majors under trusteeship or guardianship,
  • Pregnant women or lactating,
  • Minors,
  • Protected person, deprived of freedom or under justice safeguard,
  • Profiting of a medical help from government (AME),
  • Not contactable after care,
  • Patient with hepatic impairment,
  • Patient with dry mouth,
  • Patient relevant a suboptimal hearing incompatible with musicotherapy or inability to use Music-care®.

Treatment and study plan

Musicotherapy

Other

If the patient is randomized in the experimental group, he listens the Music-care® playlists and chose two closed to his musical tastes. The playlists are unique compositions create by Music-care® (french company), not known from the general public, categorized by theme (jazz, rock, world music…).

Primary outcomes

  1. Pain intensity

    Time frame: 24 hours after the dental surgery

    the pain intensity will be measured with the Visual analogue scale (VAS).

Secondary outcomes

  1. Efficacy of musicotherapy

    Time frame: 24, 48 and 72 hours

    Evaluate the anxiolytic effectiveness of " passive " musicotherapy on the reduction of peroperative anxiety during the dental surgery by STAY questionnaire

Sponsors and collaborators

Lead sponsor

Nantes University Hospital

Other

Collaborators

  • Fondation Apicil

Registry information

Official study title

Evaluation of the Effectiveness of Musicotherapy in Reducing Peroperative Anxiety and Post-surgical Pain in Dental Care

Acronym: MUSANX

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Apr 24, 2019
Registry last updated
Oct 4, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.