Comparing oral and IV fluids after knee surgery
Comparison Efficacy of Oral Fluid Versus Intravenous Fluid Replacement in Postoperative Primary Total Knee Arthroplasty : A Randomized Controlled Trial.
This study is testing whether drinking fluids or getting them through an IV helps people recover faster after knee surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 130 (estimated) |
| Ages | 40 Years to 85 Years |
| Sex | All |
| Sponsor | Thammasat University Hospital Academic / other |
| Locations | 1 site (Khlong Luang, Pathum Thani) |
| Trial ID | NCT06288815 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of oral fluid replacement versus intravenous fluid replacement in patients recovering from primary unilateral total knee arthroplasty. It will assess whether patients who receive oral fluids recover faster than those who receive IV fluids. The study will include patients aged 40 to 85 years with primary osteoarthritis and will exclude those with certain medical conditions or previous knee surgeries. The goal is to determine the optimal fluid replacement method to enhance recovery post-surgery.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 40-85 with primary osteoarthritis who are classified as ASA I or II.
Not a fit: Patients who are on diuretics, are morbidly obese, have had previous knee surgeries, or cannot undergo spinal anesthesia may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery times for patients undergoing knee surgery.
How similar studies have performed: While there may be limited data on this specific comparison, similar studies have explored fluid replacement methods in surgical recovery with varying results.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Khlong Luang, Pathum Thani
- Thammasat University — Khlong Luang, Pathum Thani, Thailand (Recruiting)
Study contacts
- Study coordinator: Yot Tanariyakul, M.D.
- Email: y.tanariyakul@gmail.com
- Phone: 663930257
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.