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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05412342
Other study ID # 43163
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date May 10, 2019
Est. completion date June 2024

Study information

Verified date December 2023
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This observational study aims to characterize the relationship between preoperative depressive symptoms and opioid use/ misuse after surgery using a perioperative learning health care system. We will follow a prospective cohort of patients undergoing elective surgery.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 687
Est. completion date June 2024
Est. primary completion date March 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Age 18+ 2. Planning to undergo surgery 3. English speaking 4. Ability and willingness to complete questionnaires and assessments Exclusion Criteria: 1. Any conditions causing inability to complete assessments (education, cognitive ability, mental status, medical status) 2. Known Pregnancy 3. Elevated Suicidality 4. Enrollment in a conflicting perioperative trial

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Stanford University School of Medicine Palo Alto California
United States Stanford Health Care Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to Opioid Cessation Assessed after surgery up to 1 year
Secondary Opioid Misuse Participant score on the Current Opioid Misuse Measure will be used to assess opioid misuse Assessed after surgery up to 1 year
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