Pain Monitoring of Herniated Disc Surgery Patients With Oura Ring

Status: Unknown
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The objective of this research study is to show whether data given by Oura ring could be used to objectively measure patients pain and well-being before and after disc surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Upcoming herniated disc surgery, ability to give a written informed concent

Locations
Other Locations
Finland
Tampere university hospital
RECRUITING
Tampere
Contact Information
Primary
Tommi Bergman, Md
tommi.bergman@pshp.fi
0331166356
Backup
Jarkko Harju, md, phd
jarkko.harju@fimnet.fi
Time Frame
Start Date: 2022-11-01
Completion Date: 2024-12-31
Participants
Target number of participants: 30
Treatments
Study group
All patients
Sponsors
Leads: Tampere University Hospital
Collaborators: Oura health oy

This content was sourced from clinicaltrials.gov