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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06288815
Other study ID # TUH oral fluid TKA
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 10, 2024
Est. completion date June 2025

Study information

Verified date March 2024
Source Thammasat University Hospital
Contact Yot Tanariyakul, M.D.
Phone 663930257
Email y.tanariyakul@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to compared efficacy of oral fluid and intravenous fluid after primary unilateral total knee arthroplasty. The main question it aims to answer is: Does oral fluid replacement after primary unilateral total knee arthroplasty provide a patient recover faster than intravenous fluids replacement?


Recruitment information / eligibility

Status Recruiting
Enrollment 130
Est. completion date June 2025
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 40 Years to 85 Years
Eligibility Inclusion Criteria: - Age 40-85 years old - ASA I, II - Primary osteoarthritis Exclusion Criteria: - Diuretics use - Morbid obesity - Previous knee surgery - Cannot undergo spinal anesthesia

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Oral fluid
Postoperation Off IV fluid immediately postoperative Allow patients drink oral fluid as protocol for 24hr
IV fluid
Postoperation IV fluid replacement as protocol for 24hr Allow patients drink oral fluid as usual

Locations

Country Name City State
Thailand Thammasat University Khlong Luang Pathum Thani

Sponsors (1)

Lead Sponsor Collaborator
Thammasat University Hospital

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

Jennings JM, Mejia M, Williams MA, Johnson RM, Yang CC, Dennis DA. The James A. Rand Young Investigator's Award: Traditional Intravenous Fluid vs. Oral Fluid Administration in Primary Total Knee Arthroplasty: A Randomized Trial. J Arthroplasty. 2020 Jun;35(6S):S3-S9. doi: 10.1016/j.arth.2020.01.029. Epub 2020 Jan 22. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time to stand and walk Stand and walk with walker Postoperative day 1
Secondary Time up and go Record time since stand up and walk 3 meters, or 10 feet away, on the floor 24 and 48 hours
Secondary Incidence of oliguria Urine output < 0.5ml/kg/hr Postoperative day 1,2
Secondary Incidence of nausea/vomiting record symptom of nausea and vomiting Postoperative day 1,2
Secondary Urine specific gravity Urine specific gravity every 4 hours Postoperative day 1
Secondary the levels of certain electrolytes Blood chemistry Postoperative day 1,2
Secondary the levels of creatinine Blood chemistry Postoperative day 1,2
Secondary the levels of blood urea nitrogen (BUN). Blood chemistry Postoperative day 1,2
Secondary Complications Pulmonary edema, heart failure, acute kidney injury Until postoperative 3months
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