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120 studies found for:    Open Studies | "Cicatrix"
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Rank Status Study
21 Not yet recruiting Study to Investigate the Pharmacokinetics, Safety, and Tolerability of BMT101 in Healthy Male Volunteers
Condition: Hypertrophic Scar
Interventions: Drug: BMT101;   Drug: Placebo
22 Recruiting Cesarean Section Scar Evaluation by Saline Contrast Sonohysterography During Hysteroscopy
Condition: Cesarean Section Scar
Intervention: Procedure: Hysteroscopic
23 Recruiting Prevalence, Risk Factors and Consequences Related to Cesarean Scar Defect (Defect in Cesarean Scar)
Condition: Cesarean Scar Defect
Intervention:
24 Recruiting Treatment of Atrophic Acne Scars With Platelet-Rich Plasma and Skin Needling
Condition: Atrophic Acne Scars
Interventions: Procedure: Platelet-Rich Plasma;   Procedure: Micro-needling
25 Recruiting Silicone Gel Versus Onion Extract Gel as Prevention for Postsurgical Scars
Condition: Hypertrophic or Keloid Scars
Interventions: Drug: Silicone gel Kelo-cort™;;   Drug: Onion extract gel Contractubex™
26 Recruiting Observational Study of Keloids Scars Treated by Shaving and Cryosurgery
Condition: Keloids Scars
Intervention:
27 Recruiting Silicone Gel to Improve Scar in Microtia Patients
Conditions: Microtia;   Scar
Intervention: Drug: Silicone Gel
28 Not yet recruiting Pilot Study to Evaluate Clinical Outcomes With the Use of Biovance Following Keloid Scar Revision Surgery
Condition: Keloid Scar
Intervention: Biological: Biovance
29 Recruiting Restylane Silk Acne Scar Efficacy Evaluation Study
Conditions: Acne;   Acne Scars;   AdverseEvent
Interventions: Device: Restylane Silk, 1.0 ml;   Device: Saline, 1.0 ml
30 Recruiting Biocellular-Cellular Regenerative Treatment Scaring Alopecia and Alopecia Areata
Conditions: Alopecia Areata;   Scarring Alopecia
Interventions: Procedure: tSVF by lipoaspiration;   Procedure: PRP Concentration;   Procedure: Emulsification tSVF;   Procedure: cSVF isolation and concentration;   Procedure: cSVF in Normal Saline IV
31 Recruiting Dose Ranging Study to Evaluate the Safety and Tolerability of SCX-001 Cream in Healthy Volunteers With Induced Dermal Incisions
Condition: Scarring
Interventions: Drug: SCX-001;   Other: Placebo
32 Not yet recruiting Efficacy of Intralesional Triamcinolone and 8% Topical Pirfenidone for Treatment of Keloid Scars
Condition: Keloid
Interventions: Drug: Topical Pirfenidone;   Drug: Triamcinolone + Pirfenidone;   Drug: Intralesional Triamcinolone
33 Recruiting Botulinum Toxin to Improve Lower Blepharoplasty Scar
Condition: Other Degenerative Disorders of Eyelid and Periocular Area
Interventions: Drug: Botulinum Toxin;   Other: Normal Saline
34 Not yet recruiting Abnormal Placenta Plant Disease Early Diagnosis and Individualized Treatment Research
Condition: Scarred Uterus
Intervention:
35 Recruiting An Exploratory Study of Genetic and Clinical Factors for Serious Skin Reactions Among Users of Eslicarbazepine Acetate
Condition: SCAR
Intervention: Other: Blood or Saliva
36 Recruiting Evaluation of the Effect of Autologous Fat and SVF Transplantation in Promoting Mechanical-stretch Induced in Vivo Skin Regeneration
Condition: Scar
Interventions: Procedure: FAT-GRAFT;   Procedure: SVF-TRANSPLANTATION;   Procedure: PLACEBO
37 Recruiting Reducing Side-effects of Autologous Skin Tissue Harvesting
Condition: Scar
Interventions: Device: Micro biopsy;   Procedure: Lidocaine with epinephrine
38 Recruiting Impact of Double-layer Versus Single-layer Uterine Closure Suture in Cesarean Section on the Development of Postoperative Uterine Scar Deficiency
Conditions: Cesarean Section;   Uterine Scar Deficiency;   Myometrial Thickness;   Single-layer Continuous Uterotomy Suture;   Double-layer Continuous Uterotomy Suture;   Transvaginal Ultrasound
Intervention: Procedure: uterine closure during cesarean section
39 Recruiting Improvement of the Appearance of Cleft Lip Scars Using Botox
Conditions: Cleft Lip;   Scarring;   Cleft Palate
Interventions: Drug: Botulinum Toxin Type A;   Drug: Normal Saline Injection
40 Not yet recruiting Psychology of Minimally Invasive Surgical Scars
Condition: Obesity
Interventions: Procedure: Standard Laparoscopic Approach;   Procedure: Percutaneous Approach

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Study has passed its completion date and status has not been verified in more than two years.