NCT06233435

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
33

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

January 23, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 31, 2024

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2025

Completed
Last Updated

September 9, 2025

Status Verified

May 1, 2025

Enrollment Period

3 months

First QC Date

January 23, 2024

Last Update Submit

September 2, 2025

Conditions

Total Knee Arthroplasty

Outcome Measures

Primary Outcomes (1)

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

    at 6 and 24 hours after total knee arthroplasty

Study Arms (2)

PADSS at 6 hours

OTHER
Behavioral: PADSS

PADSS at 24 hours

OTHER
Behavioral: PADSS

Interventions

PADSSBEHAVIORAL

Observe PADSS after total knee arthroplasty at 6 and 24 hours

PADSS at 24 hoursPADSS at 6 hours

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • Allergy to local anesthetic drugs

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Thammasat University hospital

Pathum Thani, Klong Luang, 12120, Thailand

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Prospective study
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Anesthesiology

Study Record Dates

First Submitted

January 23, 2024

First Posted

January 31, 2024

Study Start

October 1, 2023

Primary Completion

December 31, 2023

Study Completion

April 30, 2025

Last Updated

September 9, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations

TH(1)