Augmentation Clinical Trials

46 recruitingLast updated: July 25, 2026

There are 46 actively recruiting augmentation clinical trials across 22 countries. Studies span Not Applicable, Phase 2, Phase 4, Phase 1. Top locations include Cairo, Egypt, Hangzhou, Zhejiang, China, Ajman, Ajman Emirate, United Arab Emirates. Updated daily from ClinicalTrials.gov.


Augmentation Trials at a Glance

46 actively recruiting trials for augmentation are listed on ClinicalTrialsFinder across 6 cities in 22 countries. The largest study group is Not Applicable with 33 trials, with the heaviest enrollment activity in Cairo, Hangzhou, and Ajman. Lead sponsors running augmentation studies include Cairo University, Bioceramed, and GCA (Eurosilicone).

Browse augmentation trials by phase

Treatments under study

About Augmentation Clinical Trials

Looking for clinical trials for Augmentation? There are currently 2 studies actively recruiting participants. Clinical trials offer access to new treatments before they are widely available, and every approved therapy in use today was first tested through a clinical trial.

Below you can browse trials, sign up for alerts when new Augmentation trials open, and view eligibility criteria for each study. Each listing includes the study phase, locations, and enrollment details.

Frequently Asked Questions

Common questions about Augmentation clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 120 of 46 trials

Recruiting
Not Applicable

Crestal Bone Changes Following Equi-crestal Versus Subcrestal Implant Placement

Implant TherapyAugmentation, Alveolar Ridge
Misr International University28 enrolled1 locationNCT06760442
Recruiting
Not Applicable

Scaffold-guided Breast Implant Revision and Primary Breast Augmentation Surgery

Breast Augmentation ComplicationsPrimary Breast Augmentation SurgeryBreast implant revision
BellaSeno Pty Ltd87 enrolled3 locationsNCT07367698
Recruiting

The Study is an Observational Post-market Follow-up Program to Evaluate Long Term (5 Years) Safety of Mentor Breast Implants in Chinese Population

MammaplastyBreast Augmentation
Johnson & Johnson Medical (Shanghai) Ltd.6,111 enrolled4 locationsNCT06510205
Recruiting
Not Applicable

Comparison of Immediate Implant Placement With Titanium Mesh Versus Collagen Membrane in Type II Socket:

Bone AugmentationBadly Broken Maxillary Premolars Indicated for Extraction
Misr International University20 enrolled1 locationNCT06875830
Recruiting

A Post-market Prospective Clinical Study of Eurosilicone Luna Mammary Implants

Breast ReconstructionBreast AugmentationBreast Reconstruction With Silicone Implants+3 more
GCA (Eurosilicone)650 enrolled2 locationsNCT07679594
Recruiting

Post-market Prospective Clinical Study of Nagor Perle Mammary Implants

Breast ReconstructionBreast Reconstruction After MastectomyBreast Reconstruction Surgery+5 more
GCA (Eurosilicone)60 enrolled1 locationNCT06013514
Recruiting
Not Applicable

Evaluation of Lateral Sinus Floor Elevation Using Xenograft Versus L-PRF Block Combined With Xenograft

XenograftSinus Floor AugmentationMaxillary Sinus Floor Elevation+1 more
Gulf Medical University30 enrolled1 locationNCT07677007
Recruiting

Evaluation of the Safety and Performance of the Neocement® Inject P: A Prospective Observational Study in Dental Area

Bone Augmentation
Bioceramed66 enrolled1 locationNCT07179510
Recruiting

Evaluation of the Safety and Performance of the Neobone®: A Prospective Observational Study in Dental Area

Bone Augmentation
Bioceramed66 enrolled1 locationNCT07179497
Recruiting
Not Applicable

Evaluation of Multilayered PRF in Comparison With Connective Tissue Graft by Sohn Poncho's Technique on Peri-implant Mucosal Enhancement in the Esthetic Zone

Peri-implant healthSoft TissuePRF+2 more
Gulf Medical University26 enrolled1 locationNCT07649239
Recruiting
Not Applicable

Volumetric Analysis of Peri-Implant Soft Tissue Changes Between Polyethereketone(PEEK) Anatomic Healing Abutments and Standard Healing Abutments in Posterior Single Implant Restorations

Peri-implant healthPeri-Implant TissuesSoft Tissue Augmentation at Dental Implants
DR NUR HAFIZAH KAMAR AFFENDI38 enrolled1 locationNCT07624331
Recruiting
Not Applicable

Assessment of Soft Tissue Thickness Over Zygomatic Implants in Atrophied Maxilla Covered With Buccal Fat Pad vs. Palatal Pedicle Flap

Dental ImplantSoft Tissue Augmentation at Dental ImplantsZygomatic Implants+5 more
Future University in Egypt4 enrolled1 locationNCT07574606
Recruiting
Not Applicable

A Study to Evaluate the Safety and Performance of Dr Korman Laboratories' Hyaluronic Acid Filler 20 mg/mL With Lidocaine for Lip Augmentation

Lip Augmentation
Dr. Korman Laboratories Ltd.75 enrolled2 locationsNCT07204691
Recruiting

Long Term Clinical Outcome After Arthroscopic Rotator Cuff Repair Augmentation With Autologous Microfragmented Lipoaspirate Tissue

AugmentationArthroscopic Rotator Cuff RepairMicrofragmented Adipose Tissue
University of Milan52 enrolled1 locationNCT06960343
Recruiting
Not Applicable

Assessment of Soft Tissue Thickness Following Utilization of Buccal Pad of Fat Versus Platelet-rich Fibrin for Covering Zygomatic Implants: A Randomized Clinical Trial

Soft Tissue Augmentation at Dental Implants
Cairo University24 enrolled1 locationNCT07562334
Recruiting
Not Applicable

Evaluation of Tenting the Schneiderian Membrane of the Maxillary Sinus Using Titanium Mesh.

Maxillary Sinus Floor Augmentation
Suez Canal University20 enrolled1 locationNCT07035236
Recruiting

Digital Planning and Clinical Assessment of the Treated Atrophic Posterior Maxilla With a Sinus Lift Procedure: a Cross-sectional Study.

Peri-implant healthAlveolar Bone AtrophyProsthetic Complication+5 more
Saint-Joseph University100 enrolled1 locationNCT07526337
Recruiting

Impact of Alveolar Ridge Preservation on the Potential Need for Sinus Floor Elevation: A 10-year Retrospective Radiographical Study

Alveolar Bone LossAlveolar Bone AtrophyAlveolar Ridge Preservation+2 more
Saint-Joseph University130 enrolled1 locationNCT07526129
Recruiting
Not Applicable

Adjunctive Keratinized Mucosa Augmentation in Peri-Implantitis

Peri-implantitisSoft Tissue Augmentation at Dental Implants
Gazi University30 enrolled1 locationNCT07471386
Recruiting
Phase 4

Radiographical, Histomorphometrical and Biomarker Analysis After Maxillary Sinus Augmentation Utilizing Xenograft Particulate Bone Graft Mixed With Parathyroid Hormone

Maxillary Sinus Augmentation
University of Baghdad30 enrolled1 locationNCT07459075