- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04913935
Investigation of Thenar Muscles Morphometric Parameters in Patients With TMC OA
Investigation of Parameters of Trapeziometacarpal Joint Configuration and Tenar Muscles in Patients With TMC OA
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patients diagnosed with trapeziometacarpal osteoarthritis and healthy subjects will be included in the study. Thickness and cross-sectional area measurements of the thenar muscles of the patient and healthy volunteers will be performed by using Shimadzu SDU 1200-Pro ultrasound system with an 8-10 MHz linear probe. To improve the image quality and to avoid muscle compression, water immersion ultrasonography will be preferred and the hands will be positioned in a water-filled plastic container. The thenar muscles will be imaged in hands of each subject.
In this study, poster-anterior radiographic imaging will be performed. The osteoarthritis stage will be determined on the radiographic image. Three different measurements will be performed on radiography: radial subluxation of the first metacarpal base (RS), articular width (AW) of the first metacarpal, and the distance between the ulnar articular facet of the trapezium and the ulnar edge of the metacarpal (U). RS / AW ratio will be calculated.
Because TMC OA caused pain and affect performance, especially during grip activities in the osteoarthritis and control groups will be tested.
Grip strength will also be measured.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Ankara
-
Altindağ, Ankara, Turkey, 06100
- Hacettepe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with trapeziometacarpal osteoarthritis who were between 35 and 75 years
Exclusion Criteria:
- Patient with De'quervain tenosynovitis, trigger finger, entrapment neuropathy and who had undergone hand surgery were excluded.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
TMC OA
women who were diagnosed with TMC OA
|
postero-anterior radiography
Other Names:
|
Control
healty volunteer women
|
postero-anterior radiography
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ultrasound-based muscle cross-sectional area of thenar muscles in this study will investigate in TMC OA patients and healthy subjects.
Time Frame: through study completion, an average of 1 year
|
USG procedures will performed on patients with TMC OA and healthy volunteers.
Cross-sectional area measurements of thenar muscles of patient and healthy volunteers will performed using a Shimadzu SDU 1200-Pro ultrasound system with 8-10 MHz linear probe.
USG device will calibrated prior to the study.
Water bath technique for USG evaluation will preferred in order to improve the image quality and to avoid muscle compression.
The hands will positioned in a 60x50x40 cm water-filled plastic container.
Five thenar muscles will imaged in the hands of each subject: Opponens pollicis, abductor pollicis brevis, flexor pollicis brevis, first dorsal inteosseous and adductor pollicis muscles.
Images will acquired in the cross-sectional planes. 2 evaluators blinded to each other will measure 15 minutes apart.
With the first evaluator, it will measure for the second and third times at 30-minute intervals from the first measurement.
|
through study completion, an average of 1 year
|
Ultrasound-based muscle thickness of thenar muscles in this study will investigate in TMC OA patients and healthy subjects.
Time Frame: through study completion, an average of 1 year
|
USG procedures will performed on patients with TMC OA and healthy volunteers.Thickness measurements of thenar muscles of patient and healthy volunteers will performed using a Shimadzu SDU 1200-Pro ultrasound system with 8-10 MHz linear probe.
USG device will calibrated prior to the study.
Water bath technique for USG evaluation will preferred in order to improve the image quality and to avoid muscle compression.
The hands will positioned in a 60x50x40 cm water-filled plastic container.
Five thenar muscles will imaged in the hands of each subject: Opponens pollicis, abductor pollicis brevis, flexor pollicis brevis, first dorsal inteosseous and adductor pollicis muscles.
Images will acquired in the cross-sectional planes. 2 evaluators blinded to each other will measure 15 minutes apart.
With the first evaluator, it will measure for the second and third times at 30-minute intervals from the first measurement.
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The radial subluxation rate of the first metacarpal.
Time Frame: through study completion, an average of 1 year
|
In this study, while PA radiographic imaging will performed, the elbows will ppositioned in 90 ° flexion, wrists in neutral position, MCP joints at 15-20 ° flexion and nails parallel to each other.
During the scanning, patient will toush his thumbs together with maximum force.
Three different measurements will made: the radial subluxation (RS) of the first metacarpal base, the articular width of the first metacarpal (AG), and the distance between the ulnar articular facet of the trapezium and the ulnar edge of the metacarpal (U) in milimeter will measured.
RS/AG rate will calculated.
|
through study completion, an average of 1 year
|
Evaluation of functional status of hand
Time Frame: through study completion, an average of 1 year
|
Disability of Arm Shoulder and Hand (DASH) will used to determine functional status of hand.The total score is 100, and higher scores indicate a worse functional level.
|
through study completion, an average of 1 year
|
Grip strength measurement
Time Frame: through study completion, an average of 1 year
|
The grip strength will be measured in kilograms using a Jamar Hand Dynamometer
|
through study completion, an average of 1 year
|
Evaluation of functional status of hand
Time Frame: through study completion, an average of 1 year
|
Michigan Hand Outcomes Questionnaire (MHQ) includes 6 subtitles, namely general hand function, ADL, pain, work, aesthetics and satisfaction, and these headings are filled in for theight and left hand.
Score calculation for each title is calculated separately.
The total score is 100, high scores mean better functional status.
|
through study completion, an average of 1 year
|
Pain Assessment
Time Frame: through study completion, an average of 1 year
|
Pain intensity was evaluated using the visual analog scale (Visual Analogue Scale, VAS).
The patients were told that the number "0" means "no pain" and "10" means "unbearable pain" on a 10 cm horizontal line.
Patients were asked to mark the severity of pain during rest and activity on this line.
The marked place was measured and the result was recorded as the intensity of pain in cm.
|
through study completion, an average of 1 year
|
Pinch strength measurement
Time Frame: through study completion, an average of 1 year
|
The pinch strength will be measured in kilograms using a Pinchmeter.
|
through study completion, an average of 1 year
|
Minnesota hand skill test
Time Frame: through study completion, an average of 1 year
|
Hand skills are evaluated in two different ways, namely placing the discs in their slots and rotating them.
People are told that this test is a performance test and they are asked to complete the test as soon as possible.
In the insertion part of the test, the patient is asked to take the discs one by one using one hand and put them in the appropriate slots respectively.
In the rotating part of the test, the patient is asked to move the discs placed in their nests by rotating the discs in the upper right corner towards the left row.
Both tests are repeated 3 times and the result is recorded in seconds.
|
through study completion, an average of 1 year
|
9 Hole hand skill test
Time Frame: through study completion, an average of 1 year
|
This test, which is used to evaluate fine hand skills, is carried out by taking 9 pins from the ground and placing them in the holes and removing them.
The test time is approximately 10 minutes.
After the patient is told that the test is a performance test and that it will be timed, he is asked to insert the pins first and then remove them as soon as possible.
The test is performed twice consecutively on both hands and the two attempts are averaged, the results are recorded in seconds.
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: ÇİĞDEM AYHAN, ASS. PROF., Hacettepe University
Publications and helpful links
General Publications
- Wolf JM, Oren TW, Ferguson B, Williams A, Petersen B. The carpometacarpal stress view radiograph in the evaluation of trapeziometacarpal joint laxity. J Hand Surg Am. 2009 Oct;34(8):1402-6. doi: 10.1016/j.jhsa.2009.06.030. Epub 2009 Sep 10.
- Mohseny B, Nijhuis TH, Hundepool CA, Janssen WG, Selles RW, Coert JH. Ultrasonographic quantification of intrinsic hand muscle cross-sectional area; reliability and validity for predicting muscle strength. Arch Phys Med Rehabil. 2015 May;96(5):845-53. doi: 10.1016/j.apmr.2014.11.014. Epub 2014 Dec 4.
- Grechenig W, Peicha G, Weiglein A, Tesch P, Lawrence K, Mayr J, Preidler KW. Sonographic evaluation of the thenar compartment musculature. J Ultrasound Med. 2000 Nov;19(11):733-41. doi: 10.7863/jum.2000.19.11.733.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO 18/204
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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