NCT06521619

Brief Summary

This study is a retrospective analysis using the accumulated clinical database from 2017/09-2023/12 to analyze patients who underwent total knee arthroplasty and received nerve blocks. The aim is to compare the analgesic effects, incidence of nerve injury, and rate of chronic pain under different nerve block techniques.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
126

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 26, 2024

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

July 22, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 26, 2024

Completed
5 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2024

Completed
Last Updated

February 17, 2026

Status Verified

February 1, 2026

Enrollment Period

1 month

First QC Date

July 22, 2024

Last Update Submit

February 11, 2026

Conditions

Keywords

AnalgesiaNerve blockTotal knee replacement

Outcome Measures

Primary Outcomes (1)

  • Acute postoperative pain

    Acute postoperative pain

    Up to two days after surgery

Secondary Outcomes (3)

  • Range of motion

    Up to two days after surgery

  • Analgesic consumption

    Up to two days after surgery

  • Ambulation time

    Up to two days after surgery

Study Arms (2)

Patient receiving Sciatic and Femoral nerve blocks

Patient receiving Sciatic and Femoral nerve blocks

Procedure: Femoral and sciatic nerve blocks

Patient receiving Adductor canal block and infiltration of posterior capsule of knee

Patient receiving Adductor canal block and infiltration of posterior capsule of knee

Interventions

Patients receiving Adductor canal block and infiltration of posterior capsule of knee

Also known as: Adductor canal block and infiltration of posterior capsule of knee
Patient receiving Sciatic and Femoral nerve blocks

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Inclusion Criteria: * Patient receiving general anesthesia combined with nerve blocks for total knee replacement

You may qualify if:

  • Patient receiving general anesthesia combined with nerve blocks for total knee replacement

You may not qualify if:

  • Age less than 20 years old
  • Not receiving nerve blocks
  • American society of anesthesiologist physical status class greater than 4
  • Contraindicated to receiving nerve blocks

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fu Jen Catholic University Hospital

New Taipei City, 24300, Taiwan

Location

Related Publications (1)

  • Sung CH, Liu JH, Hung CF, Fu CH. Comparative analysis of adductor canal block combined with iPACK block versus femoral combined with sciatic nerve blocks: a propensity score matched study. BMC Anesthesiol. 2025 May 16;25(1):249. doi: 10.1186/s12871-025-03112-z.

MeSH Terms

Conditions

PainAgnosia

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsPerceptual DisordersNeurobehavioral ManifestationsNervous System Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Attending anesthesiologists

Study Record Dates

First Submitted

July 22, 2024

First Posted

July 26, 2024

Study Start

June 26, 2024

Primary Completion

July 31, 2024

Study Completion

July 31, 2024

Last Updated

February 17, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Patient data is protected under privacy guidelines of our institute and the need of original patient data could be obtained by written mail request to study officials and the request would be reviewed by our institute.

Locations