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Accuracy of the Transpatellar Tendon Approach to Knee Arthrocentesis

D

Denver Health and Hospital Authority

Status

Completed

Conditions

Knee Aspiration

Treatments

Procedure: Transpatellar Approach
Procedure: Suprapatellar

Study type

Interventional

Funder types

Other

Identifiers

NCT00888368
DHMC07-0387

Details and patient eligibility

About

The purpose of this study is:

  • To determine the accuracy of intraarticular placement with the transpatellar tendon approach as compared to the suprapatellar approach. Patients undergoing knee arthroscopy will be consented for study of the injection of the fluid into the joint prior to portal placement or commencement of knee replacement. Patients will be randomized to receive injections via the transpatellar tendon or superolateral approach. Using injectable contrast and fluoroscopy, the placement of injections into the knee will be evaluated for accuracy. Injection attempts with contrast fluid that uniformly coats the articular surface on sagittal and coronal radiographs will be counted as successful. A concentration of contrast fluid in extraarticular fat will be counted as a failure.

Hypothesis: The rate of accuracy of intraarticular placement of the needle tip via the transpatellar tendon approach to knee aspiration is greater than that of the superolateral approach.

  • To determine the distribution of contrast material with the transpatellar tendon and superolateral apporaches. Using a previously described evaluation technique of dividing the knee into seven compartments, sagittal and coronal fluoroscopy images will be evaluated to determine the distribution of contrast fluid.

Hypothesis: Contrast injected into the knee via the trasnpatellar tendon approach will penetrate as many compartments of the knee as contrast injected via the superolateral approach.

Enrollment

20 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • undergoing elective arthroscopic surgery of the knee
  • age greater than 18 years old and less than 80 years old
  • able to consent to a research study

Exclusion criteria

  • allergy to contrast dye, iodine or shellfish
  • currently pregnant
  • acute fracture or dislocation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

Transpatellar Approach
Experimental group
Treatment:
Procedure: Transpatellar Approach
Suprapatellar Approach
Active Comparator group
Treatment:
Procedure: Suprapatellar

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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