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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06233435
Other study ID # MTU-EC-AN-2-179/66
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 24, 2023
Est. completion date October 19, 2024

Study information

Verified date January 2024
Source Thammasat University Hospital
Contact Niruji Saengsomsuan, MD
Phone +66814295524
Email jns_owen@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 33
Est. completion date October 19, 2024
Est. primary completion date March 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
PADSS
Observe PADSS after total knee arthroplasty at 6 and 24 hours

Locations

Country Name City State
Thailand Thammasat University hospital Pathumthani Klong Luang

Sponsors (1)

Lead Sponsor Collaborator
Thammasat University Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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