Comparison of Modified Post-Anesthetic Discharge Scoring System (PADSS) Between 6 and 24 Hours in Patients Undergoing Total Knee Arthroplasty

This study is a prospective study which compares of Modified Post-Anesthetic Discharge Scoring System (PADSS) between 6 and 24 hours in patients undergoing total knee arthroplasty in Thammasat University hospital, Thailand.

Completed

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Key information

Conditions

Total Knee Arthroplasty

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Thammasat University hospital

Pathum Thani, Klong Luang, 12120, Thailand

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patient undergoing total knee arthroplasty (one side) under spinal block with adductor canal block
18-85 years old
American Society of Anesthesiologist physical status classification I-III

Exclusion criteria

Allergy to local anesthetic drugs

Treatment and study plan

PADSS

Behavioral

Observe PADSS after total knee arthroplasty at 6 and 24 hours

Primary outcomes

Comparison of Modified Post-Anesthetic Discharge Scoring System (PADSS) Between 6 and 24 Hours in Patients Undergoing Total Knee Arthroplasty

Time frame: at 6 and 24 hours after total knee arthroplasty

Sponsors and collaborators

Lead sponsor

Thammasat University Hospital

Other

Registry information

Important dates

Study start: 2023
Primary completion: 2023
Study completion: 2025
First posted: Jan 31, 2024
Registry last updated: Sep 9, 2025

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.

Completed