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Examination of Edema After Arthroscopic Shoulder Surgery

Examination of Edema After Arthroscopic Shoulder Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06014203
Enrollment
100
Registered
2023-08-28
Start date
2023-09-01
Completion date
2024-05-10
Last updated
2024-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroscopy, Edema, Shoulder

Keywords

Edema, Shoulder arthroscopy

Brief summary

The investigators's aim is to examine trunk and upper extremity edema after arthroscopic rotator cuff repair and/or labrum repair surgeries. During surgery, the shoulder joint capsule is cut and the joint is entered arthroscopically. During this procedure, approximately 3-6 liters of saline fluid is injected into the joint, depending on the duration of the surgery. The given fluid accumulates out of the joint in relation to the duration of the surgery and the amount of fluid given. In this study, the investigators aim is to examine how much the extra-articular fluid collects under the skin of the upper extremity and trunk, and the change in the amount of fluid 24 hours after surgery. Examination of the amount of subcutaneous fluid may help to better understand the postoperative complications such as edema, carpal tunnel syndrome, compartment syndrome, myolysis, and dyspnea. How much edema the joint and surrounding structures are exposed to and its relationship with the duration of surgery can help to clinicians determine the safe discharge time.

Interventions

DIAGNOSTIC_TESTEdema measurement

Subcutaneous fluid measurements will be made 3 times in total, before the surgery, immediately after the surgery and 24 hours after the surgery. Measurements will be made with the MoistureMeterD Compact local edema measuring device. Points to be measured: 1. Midpoint of the upper trapezius muscle 2. 5 cm distal to anterior acromion 3. 5cm distal to lateral acromion 4. 5cm distal to posterior acromion 5. 3cm medial to the axilla 6. Anterior cubital fossa 7. Carpal tunnel

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Arthroscopic shoulder surgery planned * 18-65 years old

Exclusion criteria

* Frozen/stiff shoulder * Metabolic and endocrine diseases * Dermatological pathologies * Hyperlaxity

Design outcomes

Primary

MeasureTime frameDescription
Edema3 monthsAfter the MoistureMeterD Compact local edema measuring device is placed perpendicular to the area to be measured, it will be held for 3 seconds and the percent moisture value will be recorded. 3 measurements will be made for each region. The average of the 3 measurements will be used in the statistical analysis.

Secondary

MeasureTime frameDescription
Surgery time3 monthsThe duration of each operation will be recorded in minutes by the surgeon performing the operation.
Amount of the saline3 monthsThe amount of saline fluid used in each operation will be recorded in liters by the surgeon performing the operation.

Countries

Turkey (Türkiye)

Contacts

Primary Contactİnci H Ayas
inciayass@gmail.com05071740342

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026