Clinical trials: Macromastia, open to volunteers
Healthy, Macromastia
NPWT Reduction Mammaplasty
In this prospective, randomized, split-body control trial, we aim to compare complications, patient-reported outcomes, and cost differentials following reduction mammaplasty with prophylactic closed incision negative pressure…
- Conditions
- Healthy, Macromastia, Negative Pressure Therapy, Mammaplasty
- Trial name
- NCT06725459
- Testing
- Prophylactic ciNPWT, Standard Adhesive Dressing
- Where
- United States
- Volunteers
- 92 people
- Sponsor
- Medstar Health Research Institute
Mammary Gland Hyperplasia
Indications for Breast Reduction in the Public Health Care System
The overall purpose of the project is to create a scientific basis for which patients should be offered breast reduction in the public sector.
- Trial name
- NCT04889469
- Testing
- Breast reduction
- Where
- Sweden
- Volunteers
- 2,000 people
- Sponsor
- Vastra Gotaland Region
Macromastia (Symptomatic)
Pectoral Block in Breast Reduction for Pain Control
A reduction mammoplasty is a commonly performed procedure for patients with symptomatic macromastia. The procedure involves removing breast parenchyma for an overall reduction in breast size and to alleviate patient symptoms…
- Trial name
- NCT07527039
- Testing
- Pectoral II Nerve Block, Post Operative Pain Relievers
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Carilion Clinic
Breast Cancer, Breast Hypertrophy
Validation of Scales in Reconstructive Breast Surgery
The main purpose of the project is to validate patient reported outcomes measures (PROMs) in reconstructive breast surgery. BREAST-Q will be evaluated for Swedish and Sweden.Hospital Anxiety and Depression Scale (HADS), EuroQol…
- Trial name
- ValPlast (NCT05233891)
- Testing
- Breast reconstruction, Breast reduction
- Where
- Sweden
- Volunteers
- 500 people
- Sponsor
- Vastra Gotaland Region
Breast Hypertrophy
ESPB Versus Intravenous Lidocaine for Pain After Mastopexy
Elective breast reduction surgery is associated with moderate-to-severe postoperative pain and a risk of developing chronic postsurgical pain.
- Trial name
- NCT07687069
- Testing
- Ultrasound - guided Erector Spine Plane Block (ESPB), Intraoperative intravenous lidocaine infusion
- Where
- Poland
- Volunteers
- 80 people
- Sponsor
- Centre of Postgraduate Medical Education
Breast Augmentation
Improved Breast Enlargement Using the Subject's Own Fat Tissue
The goal of this clinical study is to learn if the Medical Device Under Investigation (simply "the device") is safe to use in human adults undergoing breast augmentation surgery.
- Trial name
- SWIFT (NCT07869641)
- Testing
- An injectable, biodegradable hydrogel, in reconstitution medium, Reconstitution medium
- Where
- 2 sites in Belgium
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- 4Tissue