Safety and Performance of UCon Bar Electrode for the Treatment of Overactive Bladder (OAB) and Bowel Dysfunction (BD)

I

InnoCon Medical

Status

Enrolling

Conditions

Incontinence, Nighttime Urinary
Urinary Frequency More Than Once at Night
Bowel Disorders Functional
Fecal Incontinence With Fecal Urgency
Urinary Incontinence, Urge
Fecal Incontinence
Nocturia
Urinary Incontinence

Treatments

Device: UCon-Bar

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT06091566
DK_FEAS_02

Details and patient eligibility

About

UCon is a medical device for treatment of the symptoms of overactive bladder (OAB) and bowel dysfunction (BD). It electrically stimulates the DGN through the skin to obtain modulated behaviour of the bladder/bowel musculature e.g., suppress undesired bladder/bowel activity to relieve the symptoms of the patient. This clinical investigation is designed as a single-arm, prospective, multi-centre, and early feasibility study.

Full description

The overall purpose of the current clinical investigation is to evaluate the medical device with a UCon-Bar Electrode with respect to its initial safety and device performance in a cohort of 20 female patients with OAB/BD over a period of 12 weeks. The investigation consists of two periods: a screening period and an intervention period. During the screening period, the participants will be using UCon with a Patch Electrode and complete a 4 week stimulation period at home. The screening period will determine if participants fulfil the criteria to participate in the intervention period. During the intervention period, the UCon Bar Electrode will be inserted in the clitoral hood. After a recovery period (4-8 weeks), the participants will be using UCon with the Bar Electrode and complete wither a 4 week or a 12 week stimulation period at home.

Enrollment

20 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participant is female
  • Participant is ≥ 18 years of age.

Participant is diagnosed with OAB or BD.

OAB: Urinary urgency usually with one or more of the following:

i. Urinary urgency incontinence (≥1 per/week). ii. Urinary frequency (≥8 voiding/day without polyuria). iii. Nocturia (≥2 voiding/night without nocturnal polyuria).

BD: One or more of the following:

i. Faecal urgency (≥3 urgencies pr. week) together with registration of urgency in St. Mark´s and a St. Mark´s score ≥9.

ii. Faecal incontinence (urge/passive) (≥1 per/week).

Participant is able to communicate, provide feedback, understand and follow instructions during the course of the investigation, including using the device at home.

Exclusion criteria

  • Participant is medically unstable (acute illness or complication of a chronic condition, apart from the OAB or BD, that might affect the participants´ participation in the investigation).
  • Participant has an active infection in the genital area.
  • Participant has an implanted pacemaker, implantable drug pump or other active medical devices (any medical device that uses electrical energy or other sources of power to make it function).
  • Participant is pregnant, nursing or planning a pregnancy (to be confirmed with a negative pregnancy test). Women of childbearing potential must maintain effective contraception during the clinical investigation.
  • Participant is enrolled or planning to enrol in another conflicting clinical investigation or was enrolled in an investigational drug trial or medical device investigation within four weeks of enrolment.
  • Participant has neuropathy to a degree that is presumed to diminish the effect of the electrical stimulation.
  • Participant has a history of cancer in the pelvic region, are currently receiving cancer treatment, or has received radiation therapy in the pelvic region.
  • Participant has addictive behaviour defined as the abuse of alcohol, cannabis, opioids, or other intoxicating drugs.

Participant does not speak or understand Danish.

The following contraception is considered effective: Intrauterine device, hormonal contraceptives such as birth control pills, implants, contraceptive patch, vaginal ring, and contraceptive injection.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Electrical stimulation
Experimental group
Description:
Electrical stimulation to the dorsal genital nerve.
Treatment:
Device: UCon-Bar

Trial contacts and locations

0

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Central trial contact

Dianna Mærsk Knudsen

Data sourced from clinicaltrials.gov

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