Scar Formation

4

Review clinical trials related to Scar Formation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of an Intraoperative Polynucleotide Injection on Scar Quality After Thyroidectomy

The goal of this clinical trial is to learn whether a single polynucleotide injection can improve scar quality after thyroid or parathyroid surgery in adults. It will also assess the safety of the injection. The main questions this study aims to answer are the following: Does a single polynucleotide injection improve scar quality 24 weeks after surgery? Does it improve scar appearance and symptoms such as pain, itching, hardness, or tightness? Are there any side effects or wound problems related to the injection? Researchers will compare PLINEST One PN-HPT, a solution containing polynucleotides, with sterile saline, which does not contain polynucleotides. After the surgical incision is closed, participants will receive one injection along the incision line. Participants will be randomly assigned to receive either PLINEST One PN-HPT or saline. Scar healing and appearance will be checked after surgery. Formal scar assessments will be performed at 4, 12, and 24 weeks. Scar quality will be assessed using patient and researcher scar rating scales, scar measurements, photographs, symptoms, and participant satisfaction.

Participants needed: 80
Trial details
Age: 40-60Biological sex: AllType: InterventionalSponsor: Dr. Lutfi Kirdar Kartal Training and Research HospitalUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Adults aged 40 to 60 years. [+5]

Younger than 40 years or older than 60 years. [+14]

Status: Recruiting

The Effectiveness of Topical Silicone Application Combined With Photoprotection in the Development of Scarring Following Blepharoplasty

Assess the efficacy of utilizing topical silicone with photoprotection (Improscar Stick® 50) on the quality of healing following upper blepharoplasty, employing the Vancouver and POSAS scales (both patient and observer) over a minimum follow-up period of three months.

Participants needed: 30
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Instituto de Oftalmología Fundación Conde de ValencianaUpdated: Feb 4, 2026Locations: 1
Eligibility criteria

The study participants are individuals aged 18 years and older, encompassing bot...

Individuals with a history of previous surgical procedures on the eyelids, apart...

Status: Not yet recruiting

Study to Use Oral Losartan to Decrease the Risk of Postoperative Scarring Following (ACL) Reconstruction

The purpose of this study to investigate the effect of using losartan (a blood pressure lowering drug with anti-scarring properties) on preventing primary postoperative arthrofibrosis (formation of abnormal scar tissue) in the knees in participants undergoing anterior cruciate ligament (ACL) repair surgery of their knee.

Participants needed: 144
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Rush University Medical CenterUpdated: Dec 15, 2025Locations: 1
Eligibility criteria

Chondroplasty [+7]

<18 years at time of enrollment [+16]

Status: Not yet recruiting

Effect of YAP1-inhibition in Surgical Wounds.

When we get injured, our body naturally tries to heal. In adults, this healing often leads to scars - thick, stiff tissue known as fibrotic tissue. Unlike normal tissue, fibrotic tissue doesn't function properly and can cause serious health problems, depending on the affected organ. Once it forms, fibrosis is usually permanent. A good example of the fibrosis process is the healing of our skin: after a cut or surgery, the resulting scar is a type of fibrosis. Special cells called fibroblasts are key players in this process. Our study looks at a drug called verteporfin, which is already approved both in Europe and the U.S. Previous research on mice and human cells suggests it can reduce or even prevent fibrosis. We are now testing, clinically, histologically and by scRNA-seq, whether injecting verteporfin into the skin during wound healing, specifically after surgical procedures, can prevent thick, rigid scars from forming. Since the skin is easy to observe and sample, it offers a great model for studying this. Will verteporfin have an impact on how surgical wounds heal? That's what we aim to find out.

Participants needed: 24
Trial details
Phase: Phase 1, Phase 2Age: 18-55Biological sex: AllType: InterventionalSponsor: Jöri PüncheraUpdated: Apr 25, 2025
Eligibility criteria

Willing and able to provide informed consent as documented by signature [+4]

Clinical adenopathy (cervical, axillar, inguinal) defined as a lymph node of mor... [+11]