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Completed

NCT Number: NCT07686523

Acute Postoperative Pain in Outpatient UKA

This study determined or observe the acute postoperative between outpatient UKA and inpatient UKA. We observe the acute post op. at at 0,1, and 2. The acute post op pain compeared between two groups.

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Key information

Age range

45 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Boonchana Pongcharoen, Pathum Thani, Changwat Pathum Thani, Thailand

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About this study

The Oxford knee score, operative time, blood loss and moephine consumption also recored.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • age ≥ 50 years, range of movement ≥ 90°, varus deformity ≤ 10°, and flexion contracture ≤ 10°.

Exclusion criteria

  • age ≥ 75 years, ASA physical status score > 2, diagnosed obstructive sleep apnea, and intraoperative conversion to total knee arthroplasty due to full-thickness cartilage loss in the lateral compartment.

Treatment and study plan

Primary outcomes

  1. acute postoperative pain

    Time frame: at day 0 (day of surgery), day 1 and day 2

    Vas for pain, 0 to 10

Secondary outcomes

  1. Oxford knee score

    Time frame: OKS at 6 weeks, 3 months, 1 year, 2 years

    0 to 48 points

Sponsors and collaborators

Lead sponsor

Thammasat University

Other

Registry information

Official study title

Acute Postoperative Pain in Outpatient Versus Inpatient Unicompartmental Knee Arthroplasty: A Prospective Cohort Study

Acronym: Outpatient UKA

Important dates

Study start
2022
Primary completion
2024
Study completion
2025
First posted
Jul 7, 2026
Registry last updated
Jul 7, 2026

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.

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