Examining fluid buildup after shoulder surgery
Examination of Edema After Arthroscopic Shoulder Surgery
This study looks at how much fluid builds up under the skin after shoulder surgery to see if it relates to the surgery time and the amount of fluid used.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Gazi University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06014203 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the accumulation of fluid in the trunk and upper extremity following arthroscopic shoulder surgeries, specifically rotator cuff and labrum repairs. During these procedures, saline fluid is injected into the shoulder joint, and the study will measure how much fluid collects under the skin in relation to the surgery's duration and the volume of fluid used. By assessing the amount of subcutaneous fluid, the researchers hope to gain insights into potential postoperative complications such as edema and other related conditions. The study will track changes in fluid accumulation 24 hours post-surgery to better understand these effects.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 18-65 who are scheduled for arthroscopic shoulder surgery.
Not a fit: Patients with frozen shoulder, metabolic or endocrine diseases, dermatological pathologies, or hyperlaxity may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management of postoperative complications related to fluid accumulation.
How similar studies have performed: While there may be studies on postoperative edema, this specific examination of fluid accumulation in relation to arthroscopic shoulder surgery is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Arthroscopic shoulder surgery planned * 18-65 years old Exclusion Criteria: * Frozen/stiff shoulder * Metabolic and endocrine diseases * Dermatological pathologies * Hyperlaxity
Where this trial is running
Ankara
- Gazi University — Ankara, Turkey (Recruiting)
Study contacts
- Study coordinator: İnci H Ayas
- Email: inciayass@gmail.com
- Phone: 05071740342
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.