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CompletedNCT01450904Updated Oct 12, 2011

The Recovery Time of Quadriceps Strength After Total Knee Arthroplasty (TKA): The Effect of Quadriceps Incision Length

An interventional study of Quadriceps incision < 2 cm and Quadriceps incision 2-4 cm in Osteoarthritis of Knee, sponsored by Mahidol University. Completed. Open to participants aged 40 Years to 85 Years. Per ClinicalTrials.gov, last updated 2011-10-12.

Sponsored by Mahidol University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
40 Years to 85 Years
Sex
All
01

Study summary

Minimally invasive total knee arthroplasty (MIS-TKA) became the popular technique. It had the less postoperative pain and shorter recovery time compared to the conventional technique. With using MIS technique, less cut of quadriceps tendon was the key. It related to keep more quadriceps strength and improve functional performance after TKA. However, there was no previous studies about the effect of quadriceps incision length in the recovery time of the quadriceps strength. The investigators hypothesized that longer quadriceps incision affected the longer recovery time of quadriceps strength in MIS-TKA.

02

Conditions studied

  • Osteoarthritis of Knee
03

In context

Osteoarthritis, Knee

3,302 studies on the registry are indexed under Osteoarthritis, Knee; 608 are open to participants now.

This study's enrollment of 60 is below the median of 70 across 2,731 interventional studies indexed under Osteoarthritis, Knee.

Browse Osteoarthritis, Knee studies →

Lead sponsor

Mahidol University is the lead sponsor of 730 studies on the registry; 118 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • The patients who diagnosed primary osteoarthritis of knee with

    1. varus or valgus deformity \< 20 degrees
    2. preoperative range of motion > 90 degrees
    3. extension lag \< 10 degrees
    4. Flexion contracture \< 30 degrees

Exclusion criteria

Exclusion Criteria:

  • Bilateral simultaneous total knee arthroplasty
  • Previous knee surgery
  • Inadequate exposure during the surgery
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Group A

    The length of Quadriceps incision was less than 2 cm.

    Procedure: Quadriceps incision < 2 cm

  • Experimental
    Group B

    The length of Quadriceps incision was 2 to 4 cm.

    Procedure: Quadriceps incision 2-4 cm

  • Experimental
    Group C

    The length of Quadriceps incision was more than 4 cm.

    Procedure: Quadriceps incision > 4 cm

Interventions

  • ProcedureQuadriceps incision < 2 cm

    MIS-TKA was performed with less than 2 cm Quadriceps incision length

  • ProcedureQuadriceps incision 2-4 cm

    MIS-TKA was performed with 2 to 4 cm Quadriceps incision length

  • ProcedureQuadriceps incision > 4 cm

    MIS-TKA was performed with more than 4 cm Quadriceps incision length

06

What researchers measure

Primary outcomes

  1. The recovery time of Quadriceps strength

    Quadriceps strength was tested every month postoperatively, Recovery time was the amount of months which the Quadriceps strength returned to preoperative level.

    Time frame: Upto 6 months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01450904
Lead sponsor
Mahidol University
Responsible party
Sponsor
First posted
Oct 12, 2011
Start date
Apr 2011
Primary completion
Oct 2011
Completion
Oct 2011
Last update
Oct 12, 2011

Study contacts

Keerati Charoencholvanich, MD
principal investigator · Mahidol University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2011. You cannot join it, but the record below documents what was studied.

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