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Feasibility of short-term temporary discontinuation of serotonin reuptake inhibitors in patients planned for hip or knee arthroplasty

Status
Withdrawn
Phases
Phase 3Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-509988-24-00
Enrollment
100
Registered
2024-03-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Hip and knee osteoarthritis

Brief summary

The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who are able to discontinue SSRI/SNRI therapy perioperatively.

Detailed description

The proportions of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who opt out of the tapering of SSRI/SNRI therapy due to discontinuation syndrome, relapse of depression, relapse of anxiety or other reasons., The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who are not able to discontinue SSRI/SNRI therapy completely, but able to reduce their doses., Discontinuation-Emergent Signs and Symptoms (DESS), Major Depression Inventory (MDI) and Symptom Checklist 92 (SCL-92) score at baseline, after 2 weeks, the day before surgery (after 5 weeks) and 2 months after surgery., The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who uses SSRIs/SNRIs 2 months after surgery., The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy able to discontinue SSRI/SNRI therapy perioperatively who uses SSRIs/SNRIs 2 months after surgery.

Interventions

DRUGDULOXETINE
DRUGSERTRALINE
DRUGPAROXETINE
DRUGESCITALOPRAM
DRUGCITALOPRAM

Sponsors

Sygehus Lillebaelt Vejle Sygehus
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who are able to discontinue SSRI/SNRI therapy perioperatively.

Secondary

MeasureTime frame
The proportions of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who opt out of the tapering of SSRI/SNRI therapy due to discontinuation syndrome, relapse of depression, relapse of anxiety or other reasons., The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who are not able to discontinue SSRI/SNRI therapy completely, but able to reduce their doses., Discontinuation-Emergent Signs and Symptoms (DESS), Major Depression Inventory (MDI) and Symptom Checklist 92 (SCL-92) score at baseline, after 2 weeks, the day before surgery (after 5 weeks) and 2 months after surgery., The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy, who uses SSRIs/SNRIs 2 months after surgery., The proportion of patients planned for THA/TKA/UKA in SSRI/SNRI therapy able to discontinue SSRI/SNRI therapy perioperatively who uses SSRIs/SNRIs 2 months after surgery.

Countries

Denmark

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026