Acute Postoperative Pain in Outpatient UKA | NCT07686523

Studies
Acute Postoperative Pain in Outpatient UKA

NCT07686523

Sponsor

Thammasat University

Status

Completed

Last Update Posted

Jul 7, 2026Actual

Enrollment

244Actual

Phase

Not provided

Conditions

Acute Post Operative Pain

Interventions

Not provided

Countries

Thailand

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Jan 2022

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 1, 2022Actual

Primary Completion Date

Oct 24, 2024Actual

Completion Date

Jan 1, 2025Actual

First Submitted Date

Jun 23, 2026

First Submission Date that Met QC Criteria

Jul 3, 2026

First Posted Date

Jul 7, 2026Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Jul 3, 2026

Last Update Posted Date

Jul 7, 2026Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Yes

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

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.

Detailed Description

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

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

244Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Inpatient UKA		Aii patients received the stabndard surgical technique.
outpatient UKA		all patients received the standard surgical technqiue

Interventions

Not provided

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
acute postoperative pain	Vas for pain, 0 to 10	at day 0 (day of surgery), day 1 and day 2

Secondary Outcomes

Measure	Description	Time Frame
Oxford knee score	0 to 48 points	OKS at 6 weeks, 3 months, 1 year, 2 years

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

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.

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

45 Years

Maximum Age

75 Years

Standard Ages

AdultOlder Adult

Study Population

anteromedia osteoarthritis of the knee

Sampling Method

Non-Probability Sample

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Not provided

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Boonchana Pongcharoen		Pathum Thani	Changwat Pathum Thani	12120	Thailand
Faculty of medicine, Thammsat university

IPD Sharing Statement Module

Plan to Share IPD

Description

IPD will not be shared, or why a decision has not been made yet.

Types

Not provided

Time Frame

Not provided

Access Criteria

Not provided

URL

Not provided

Condition Browse Module

MeSH Terms

ID	Term
D010149	Pain, Postoperative

Ancestor Terms

ID	Term
D011183	Postoperative Complications
D010335	Pathologic Processes
D013568	Pathological Conditions, Signs and Symptoms
D010146	Pain

Browse Leaves

Not provided

Browse Branches

Not provided