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Paraffin Oil for Preventing Tourniquet-Related Skin Lesions in Upper Extremity Surgery (PARA-TOUR RCT)

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This randomized controlled trial aims to evaluate the effectiveness of topical paraffin oil application in preventing tourniquet-related skin lesions in patients undergoing upper extremity surgery. Pneumatic tourniquets are commonly used to provide a bloodless surgical field; however, they may cause skin complications such as erythema, edema, abrasions, blisters, and burns. In this study, adult patients undergoing elective upper extremity surgery will be randomly assigned to either an intervention group receiving topical paraffin oil application in addition to routine protective dressing or a control group receiving routine care only. Skin integrity will be assessed immediately after tourniquet removal and at 30 and 60 minutes postoperatively using standardized skin assessment criteria. The findings of this study are expected to contribute to the development of effective, simple, and cost-efficient strategies to prevent tourniquet-related skin complications and improve patient safety and postoperative comfort.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years

• Patients scheduled for elective upper extremity surgery requiring pneumatic tourniquet application

• ASA physical status I-III

• Body mass index (BMI) \<30 kg/m²

• Ability to provide informed consent

• Willingness to participate in the study

Locations
Other Locations
Turkey
Kartal Dr. Lütfi Kırdar City Hospital Istanbul, Turkey
RECRUITING
Istanbul
Contact Information
Primary
Muzeyyen Ataseven, PhD, RN
muzeyyenataseven@hotmail.com
+90 505 229 9474
Time Frame
Start Date: 2026-01-12
Estimated Completion Date: 2026-06
Participants
Target number of participants: 90
Treatments
Experimental: Paraffin Oil Group
Participants receive topical paraffin oil application before tourniquet placement in addition to routine protective dressing.
No_intervention: Control Group
Participants receive routine protective dressing without paraffin oil application.
Related Therapeutic Areas
Sponsors
Collaborators: Medipol University, Kartal Dr. Lütfi Kirdar City Hospital
Leads: Istanbul Medipol University Hospital

This content was sourced from clinicaltrials.gov