Clinical trials for cosmetic silicone injections

Find a study all fields optional Saved Studies. Recruiting and not yet recruiting studies All studies. Condition or disease For example: breast cancer x.

Other terms For example: NCT number, drug name, investigator name x. Yemen Zambia Zimbabwe x. City x. Distance 50 miles miles miles miles. The purpose of this study is to investigate outcomes for all patients with upper or lower extremity lymphedema with lymph node transfer in a two stage procedure involving dermal regeneration followed by split thickness skin graft STSG and compared to patients only receiving STSG for wound coverage.

The purpose of this study is to collect skin that is clinical residue and would be otherwise discarded for research purposes with proper patient consent. The purpose of this study is to determine whether administration of Topical Transexamic Acid TXA at the time of tissue expander placement in the setting of implant-based breast reconstruction reduces postoperative drain volume, as well as reducing the time until drains meet criteria for removal. The purpose of this study is to assess outcomes, satisfaction and aesthetics of two different breast reconstruction techniques Goldilocks alone, and Goldilocks with Implant-Based Reconstruction and compare its safety, patient satisfaction, aesthetic evaluation and complications.

The primary purpose of this study is to identify the therapeutic effect of Adipose-Induced Regeneration AIR in radiation-induced skin injury of post-mastectomy breast cancer patients. Keeping these issues in mind we planned to study an alternative option i. When doing the literature review the investigator found scanty evidence so the investigator decided to perform this RCT.

FDA Resources. Arms and Interventions. It is self-adhesive sheet made from medical graded Silicone. After explaining and taking consent from the patient about the intervention, pre- intervention assessment will be made. Final assessment will be made after 3 months of first intervention.

Derma Pen is an electric device, used for microneedling. These needles penetrate the skin upto 2mm. Outcome Measures. Primary Outcome Measures : Cosmetic Outcome [ Time Frame: 3 Months ] It will be assessed using, Vancouver scar scale at time of presentation and at 3 months after the intervention.

Eligibility Criteria. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision.

Patients who received treatment for keloids or hypertrophic scar in past. Patients with active inflammation in area of hypertrophic scar or in its vicinity. Contacts and Locations. Information from the National Library of Medicine 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. More Information. National Library of Medicine U. National Institutes of Health U. Department of Health and Human Services. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Hypertrophic Scar.

Not Applicable. Study Type :. Interventional Clinical Trial. Estimated Enrollment :.