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Active clinical trials for "Cicatrix"

Results 141-150 of 238

3-D Imaging Assessment of Scar Formation and Would Healing in Fat Grafted vs Non-Fat Grafted Facial...

Scar FormationAutologous Fat Grafting

The purpose of this study is to assess scar-formation and wound healing following the use of autologous fat grafting in facial reconstruction patients. Patients who have undergone facial reconstruction in the last 3 months will be randomized into two groups, one receiving fat grafting and one not receiving any intervention. These patients will continue to follow-up in our clinic for one year, with 3-D images taken at each follow-up visit to assess scar formation and wound healing. Assessment of the scar will be undertaken by both healthcare personnel as well as general lay public. We hypothesize that patients undergoing fat grafting to the wound site will achieve a more aesthetically appealing result, with less scarring and improved wound healing as judged by both the general public and healthcare professionals.

Withdrawn5 enrollment criteria

Juvista (Avotermin) in Scars Following Varicose Vein Removal

Varicose VeinsCicatrix

This trial is being undertaken to investigate the efficacy and safety of Juvista in the improvement of scar appearance when administered to approximated wound margins following varicose vein surgery. The results from this trial will be used to select doses for investigation in future clinical trials with the compound.

Completed18 enrollment criteria

RN1001(Avotermin) in Scar Improvement Following Breast Augmentation

MammaplastyCicatrix

This will be a multi-centre, double-blind, within-subject, placebo controlled randomised trial in female subjects. All subjects will undergo bilateral breast augmentation surgery. Immediately following surgery, each subject will receive 100µl containing 50ng or 200ng of RN1001 per linear centimetre intradermally into both margins of one breast wound, and 100µl of placebo solution per linear centimetre intradermally into both margins of their other breast wound. The allocation of treatment to wound (left or right) will be randomised and double blind.

Completed20 enrollment criteria

Juvista in Scar Revision Surgery of Disfiguring Scars

Cicatrix

This trial is to determine whether Juvista can prevent scar formation or improve the appearance of scars following scar revision surgery. The trial will involve comparing Juvista to placebo.

Completed34 enrollment criteria

Aquatic Training in Patients With Severe Scarring

BurnsScar

Aim: - to investigate the effects of an aquatic exercise program in patients with severe scars Patient population: 10 patients of at least 18 years old patients with scars after burns or other severe skin injuries stratification into two groups: an intervention group and a control group Method: 8 patients will participate in the aquatic exercise group and 2 patients in the control group assessment of physical fitness parameters, scar tissue and psychosocial impact Hypothesis: - patients of the aquatic exercise group will recover sooner and better (physically and psychologically) than patients of the control group

Withdrawn5 enrollment criteria

Safety and Efficacy of Umbilical Cord Mesenchymal Stem Cell Local Intramuscular Injection for Treatment...

Uterine Scar

This is a single center, randomized, double blind, placebo controlled study to evaluate the safety and efficacy of umbilical cord mesenchymal stem cell local intramuscular injection for treatment of caesarean section uterine scars.

Withdrawn14 enrollment criteria

Safety of Umbilical Cord Mesenchymal Stem Cell Local Intramuscular Injection for Treatment of Uterine...

Uterine Scar

The purpose of this study is to evaluate the safety of umbilical cord mesenchymal stem cell local intramuscular injection for treatment of uterine scars by a prospective, single-center, open, and single-arm clinical trial.

Withdrawn14 enrollment criteria

: Protescal: Prevention of Hypertrophic Scar and Keloid Formation Post Caesarean Section

Caesarean WoundHypertrophic Surgical Scar1 more

This study aimed to evaluate the effectiveness of Protescal in preventing post caesarean section hypertrophic scar and keloid formation.

Completed4 enrollment criteria

Early Intervention With Non-ablative Fractional Laser to Reduce Cutaneous Scarring

Cicatrix

To investigate intervention with early application of non-ablative laser to prevent scarring in the skin

Completed10 enrollment criteria

Fractional Laser Therapy and Dermabrasion for Scar Revision

Scar

The goals of this study will be to compare the safety and efficacy of fractional photothermolysis (Fraxel) with dermabrasion when used for scar revision.

Withdrawn13 enrollment criteria
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