Efficacy of Platelet Rich Plasma Injection Plus Fat Grafting as Compared to Fat Grafting Alone on Burn Scar by Using Vancouver Scar Scale
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| ClinicalTrials.gov Identifier: NCT04781348 |
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Recruitment Status :
Not yet recruiting
First Posted : March 4, 2021
Last Update Posted : March 5, 2021
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Background: - Burn injuries always leave behind some permanent marks on the body of a victim. For the treatment of these scars, digital photography along with scar scales instrument are an important instrument for the patient's evaluation and finally for the follow-up of scars. Clinical evaluation of the patient after the use of Platelet concentration that it is a beneficial treatment which affects both on hard and soft tissues healing because of having growth factors deposited in PRP. Therefore, it can be used as an alternative to surgery which promotes safe and natural healing in such patients.
Objectives: -
1. To determine the efficacy of Platelet Rich Plasma plus fat grafting as compared to fat grafting alone on the Vancouver scar scale.
Methodology: - An experimental controlled comparison trial study will be done on burn patients, admitted for recovery at the Plastic surgery department, Civil Hospital Karachi after the approval of the scientific committee and Institutional review board of Dow University of Health Sciences, Karachi. The study participants fulfilling the inclusion criteria giving consent will be randomly divided into two groups, one group will receive only fat grafting whereas another group will receive Platelet Rich Plasma plus fat grafting. The sample size of the study will be 52(26 in each group). Both the groups will be followed initially for 15 days of two visits then monthly two visits and finally after 6 months. Assessment of scar with Vancouver Scars Scale (VSS) will be done. The association of the PRP plus fat cells group and control group will be done by applying Chi-square statistical test. P-Value will be set for statistical significance level at <0.05.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Burn | Procedure: Platelet Rich Plasma plus fat grafting | Phase 4 |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 1 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Treatment |
| Official Title: | Efficacy of Platelet Rich Plasma Injection Plus Fat Grafting as Compared to Fat Grafting Alone on Burn Scar by Using Vancouver Scar Scale |
| Estimated Study Start Date : | March 1, 2021 |
| Estimated Primary Completion Date : | April 15, 2021 |
| Estimated Study Completion Date : | September 28, 2021 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Platelet Rich Plasma plus fat grafting
Group will receive Platelet Rich Plasma plus fat grafting
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Procedure: Platelet Rich Plasma plus fat grafting
The study participants fulfilling the inclusion criteria giving consent will be randomly divided into two groups, one group will receive only fat grafting whereas another group will receive Platelet Rich Plasma plus fat grafting. |
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Experimental: Fat grafting
Group will receive only fat grafting
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Procedure: Platelet Rich Plasma plus fat grafting
The study participants fulfilling the inclusion criteria giving consent will be randomly divided into two groups, one group will receive only fat grafting whereas another group will receive Platelet Rich Plasma plus fat grafting. |
- Assessment of change in scar [ Time Frame: Both the groups will be followed initially for 15 days of two visits then monthly two visits and finally after 6 months. ]Assessment of scar with Vancouver Scars Scale
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| Ages Eligible for Study: | 18 Years to 60 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- All the buns patients of either age or sex coming with burn scar for plastic surgery.
- Give consent for this study
- Aesthetically not pleasant
- Exposed body parts
- Mature scar
Exclusion Criteria:
- Immature scar
- Systematic illness.
- Sepsis
- Psychiatric illness.
- Pregnant women
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04781348
| Contact: Nasreen Bano, MBBS | 92-21-3312278136 | nishokhatri@gmail.com |
Other Publications:
| Responsible Party: | Nasreen Bano, Dr., Dow University of Health Sciences |
| ClinicalTrials.gov Identifier: | NCT04781348 |
| Other Study ID Numbers: |
1957 |
| First Posted: | March 4, 2021 Key Record Dates |
| Last Update Posted: | March 5, 2021 |
| Last Verified: | March 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Platelet-rich plasma Fat grafting Efficacy |
wound healing Burns scar Regeneration |
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Burns Wounds and Injuries |

