Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT07057557

Aloe Vera vs Paraffin Tulle Dressings for Pain Management in Split Thickness Skin Graft Donor Sites

Led by King Edward Medical University · Updated on 2025-09-25

72

Participants Needed

1

Research Sites

36 weeks

Total Duration

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AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if Aloe Vera gel dressing helps reduce pain better than traditional paraffin-based tulle dressing at the donor site of split-thickness skin grafts in adult patients aged 18 to 60. The main questions it aims to answer are: Does Aloe Vera gel dressing reduce postoperative pain more effectively than paraffin-based tulle dressing on the 7th day after surgery? Is there a difference in the need for additional pain medication between the two groups? Researchers will compare Aloe Vera gel dressing to paraffin-based tulle dressing to see if Aloe Vera leads to better pain control. Participants will: Undergo split-thickness skin graft surgery Receive either Aloe Vera gel dressing or paraffin-based tulle dressing at the donor site Have pain measured using a visual analogue scale (VAS) on the 7th day after surgery Be given pain medication if their pain score is 4 or higher, and the amount used will be recorded

CONDITIONS

Official Title

Aloe Vera vs Paraffin Tulle Dressings for Pain Management in Split Thickness Skin Graft Donor Sites

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 60 years of either gender needing split-thickness skin graft
Not Eligible

You will not qualify if you...

  • Patients with altered pain response due to conditions like diabetes, neuropathy, chemotherapy, or opioid use
  • Patients allergic to Aloe Vera gel or paraffin-based tulle dressings

AI-Screening

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Trial Site Locations

Total: 1 location

1

Mayo Hospital Lahore

Lahore, Punjab Province, Pakistan

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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