Ozmosi | BTL EMSELLA Drug Profile
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BTL EMSELLA

Alternative Names: BTL EMSELLA
Clinical Status: Inactive
Latest Update: 2025-12-11
Latest Update Note: Clinical Trial Update

Product Description

BTL EMSELLA uses HIFEM technology for PFM strengthening and reduction of UI. The device is consisted of a power generator and a circular coil mounted in the seat of the chair.  (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016513/)

Mechanisms of Action: No Mechanism

Novel Mechanism: No

Modality: Unknown

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: Colombia

Approved Indications: None

Known Adverse Events: None

Company: William Beaumont Hospitals
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT04873037

EmsellaOAB

N/A

Recruiting

Overactive Bladder

2028-06-01

2025-12-12

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

NCT04133675

NCT04133675

N/A

Recruiting

Urinary Incontinence, Stress|Enuresis

2027-10-01

2024-11-08

NCT05370651

Emsella_EJD

N/A

Recruiting

Erectile Dysfunction|Pelvic Pain|Aging, Premature|Premature Ejaculation|Liver Failure

2027-07-01

2025-12-12

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

NCT04031014

NCT04031014

N/A

Completed

Overactive Bladder|Urinary Incontinence, Stress|Urinary Incontinence, Urge

2025-07-01

2025-09-06

Primary Endpoints|Treatments|Trial Status

NCT03877640

BTL EMSELLA

N/A

Unknown status

Urinary Incontinence, Urge|Urinary Incontinence, Stress

2024-06-01

2025-11-01

Primary Endpoints|Treatments|Trial Status

NCT04248491

EmsellaPain

N/A

Terminated

Pelvic Pain

2023-01-18

2023-09-22

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date

NCT04138602

NCT04138602

N/A

Withdrawn

Fecal Incontinence

2020-09-01

2020-09-10

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

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