A Study to Evaluate the Safety and Initial Efficacy of a Novel Intrauterine Device

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Szőczei Beáta, MD, Synexus
ClinicalTrials.gov Identifier:
NCT01590563
First received: April 20, 2012
Last updated: July 29, 2013
Last verified: July 2013
  Purpose

Current intrauterine devices (IUD) pose such risks as uterine perforation during insertion, malposition and expulsion. The investigated device, the IUB(tm) SCu300A is an IUD which is inserted in a similar fashion into the uterus and takes a three dimensional spherical shape while curving away from the fundus. Apart for an anticipated reduction in the rate of stated complications, its smaller size and mallable characteristics are also expected to improve user experience. The clinical trial is intended to evaluate the safety and initial efficacy of this novel device.


Condition Intervention Phase
Contraception.
Device: Intrauterine device
Phase 1

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: A Study to Evaluate the Safety and Initial Efficacy of a Spherical Copper Intrauterine Contraceptive Device the IUB(tm)

Further study details as provided by Ocon Medical Ltd.:

Primary Outcome Measures:
  • Comparable or reduced rates of uterine perforation [ Time Frame: During installation ] [ Designated as safety issue: Yes ]
    Uterine perforation is an established risk of IUD deployment which may cause certain health hazards. It is anticipated that the IUB(tm), through its form and deployment pattern, will reduce this risk.

  • Efficacy in preventing pregnancy [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Prevention of pregnancy will be measured. Pregnancy rates are expected to be comparable to current IUDs.


Secondary Outcome Measures:
  • Comparable or reduced occurence of malposition, expulsion, change in bleeding pattern and pain. [ Time Frame: 12 months ] [ Designated as safety issue: No ]
    Expulsion and malposition are established risks involved with IUD use. Occurance of these risks may drastically reduce effectiveness. Change in bleeding patterns and pain incurred by the patient are also known side effects which affect patient quality of life and may result in IUD removal. It is expected that the IUB(tm) form will reduce these risks and side effects.


Enrollment: 15
Study Start Date: April 2012
Study Completion Date: July 2013
Primary Completion Date: July 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: SCu300A IUB Device: Intrauterine device
Insertion of a spherical IUD, one year follow-up
Other Name: SCu300A IUB(tm)

Detailed Description:

A copper IUD (intrauterine device or coil) is a type of intrauterine contraceptive device. Most IUDs have a plastic T-shaped frame which is wrapped in copper wire and sleeves. The device has to be fitted inside and removed from the uterine cavity by a doctor or qualified medical practitioner. It remains in place the entire time pregnancy is not desired.

The IUD is a long acting reversible contraceptive, with different IUDs intended to last for different lengths of time, usually between 3 and 10 years. The length of time that the device lasts depends mainly on the amount of exposed copper, which is indicated, in square millimeters, by a number in the name of each device (i.e., the Paragard T-380A has 380 square millimeters of exposed copper).

The IUD is the world's most widely used method of reversible birth control, currently used by over 175 million women.

The mechanism of IUDs is not well understood. It is known however that the presence of a device in the uterus prompts the release of leukocytes and prostaglandins by the endometrium. These substances are hostile to both sperm and eggs; the presence of copper increases the spermicidal effect. The general medical consensus is that spermicidal and ovicidal mechanisms are the only way in which IUDs work. Some physicians and medical texts have suggested they may have a secondary effect of interfering with the development of pre-implanted embryos; this secondary effect is considered more plausible when the IUD is used as emergency contraception.

Second-generation copper-T IUDs have failure rates of less than 1% per year, and cumulative 10-year failure rates of 2-6%. A copper IUD may also be used as emergency contraception. If an IUD is inserted within five days of unprotected intercourse, a woman's chance of pregnancy is reduced to that of ongoing IUD users.

IUDs do not protect against STDs or PID.

Made from a shape memory alloy of a specific size and shape, the SCu300A IUB™ is inserted through an insertion tube much like regular IUDs, however, when pushed out, in the uterus, it takes a spherical shape. An important feature includes its downwards curving opposite to the uterine fundus as it emerges out of the tube, minimizing the risk of perforation. The three dimensional shape's elasticity allows for better amenability to the uterus, nullifying the possibility of malposition and its final outer diameter reducing the probability of expulsion. Lacking rigid or protruding segments and being significantly smaller than other IUDs, the IUB™ is expected to reduce distortion and tissue irritation, possibly resulting in less bleeding, discomfort and pain, leading to lower discontinuation rates. A thread is attached to the IUB™ to allow easy removal.

The trialed IUB™ will be copper-based (Cu surface area of 300mm2).

This study aims to assess the IUB™'s safety and initial efficacy. Endpoints include the assessment of changes in discomfort, pain and menorrhea, changes in the endometrium discontinuation rates as well as user experience. These results will be used as regulatory evidence and will also help in reaffirming the assumption that the IUB™'s design contributes to lower complication and side effect rates.

  Eligibility

Ages Eligible for Study:   25 Years to 42 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Adult female aged 25-42
  • Free willing to fully comply with treatment process
  • Healthy women
  • Married or in a steady relationship. Blood hemoglobin >11.5gr%
  • Signed informed consent form

Exclusion Criteria:

  • Pregnancy or suspicion of pregnancy
  • Use of other contraception methods
  • Abnormalities of the uterus resulting in distortion of the uterine cavity
  • Acute current or past history of pelvic inflammatory disease, or current behavior suggesting a high risk for pelvic inflammatory disease
  • Postpartum endometritis or postabortal endometritis in the past 3 months
  • Known or suspected uterine or cervical malignancy
  • Genital bleeding of unknown etiology
  • Mucopurulent cervicitis
  • Wilson's disease
  • Allergy to any component of IUB™
  • A previously placed IUD that has not been removed
  • Known intolerance or allergy to copper and/or copper IUDs
  • Medication that may interfere with the subject's ability to complete the protocol
  • Any other significant disease or condition that could interfere with the subject's ability to complete the protocol
  • A history of alcohol or drug abuse
  • known infection with human immunodeficiency virus (HIV), Hepatitis B or Hepatitis C
  • Planned pregnancy during the follow-up period
  • Participation in another clinical trial
  • Anemia of any kind or blood hemoglobin lower than 11.5gr%.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01590563

Locations
Hungary
Synexus Hungary Limited
Budapest, Hungary, 1036
Sponsors and Collaborators
Ocon Medical Ltd.
Investigators
Principal Investigator: Beata Szoczei, MD Synexus Hungary Kft.
  More Information

No publications provided by Ocon Medical Ltd.

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Szőczei Beáta, MD, Medical Doctor, Synexus
ClinicalTrials.gov Identifier: NCT01590563     History of Changes
Other Study ID Numbers: AOS-C1000-02
Study First Received: April 20, 2012
Last Updated: July 29, 2013
Health Authority: Hungary: Scientific and Medical Research Council Ethics Committee

ClinicalTrials.gov processed this record on October 01, 2014