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Cervical Device Contraception-2 (Nanopaz) (NANOPAZ)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00689494
Recruitment Status : Unknown
Verified June 2008 by Bnai Zion Medical Center.
Recruitment status was:  Not yet recruiting
First Posted : June 3, 2008
Last Update Posted : June 3, 2008
Information provided by:
Bnai Zion Medical Center

Brief Summary:
Measure blood progesterone by using cervical device contraception.

Condition or disease Intervention/treatment Phase
Healthy Other: Nanopaz contraception device Phase 1 Phase 2

Detailed Description:

A very small cervical device that releases small amount of progesterone 20 mcgm/day.

The target of the research is to measure blood progesterone by using the cervical device.

This small device delivers progesterone by nanotechnology method.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 10 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Cervical Device Contraception
Study Start Date : June 2008
Estimated Primary Completion Date : December 2008
Estimated Study Completion Date : May 2010

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Birth Control

Intervention Details:
  • Other: Nanopaz contraception device
    levonorgestrel and levonorgestrel device for cervical contraception-nantechnolgy method
    Other Name: levonorgestrel device for cervical contraception-nantechnolgy method

Primary Outcome Measures :
  1. blood progesterone measure in blood [ Time Frame: one to two months ]

Information from the National Library of Medicine

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Ages Eligible for Study:   1 Month to 2 Months   (Child)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • 10 healthy women are candidate for hysterectomy

Exclusion Criteria:

  • Women with neoplastic malignancy disease or thrombophylia

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Responsible Party: Baram Paz, Bnai Zion MC Identifier: NCT00689494    
Other Study ID Numbers: BnaiZionMC-08-BP-003-CTIL
First Posted: June 3, 2008    Key Record Dates
Last Update Posted: June 3, 2008
Last Verified: June 2008
Keywords provided by Bnai Zion Medical Center:
Nanopaz device
Blood progesterone measure in using the device
Delivery progesterone
Progesterone levonorgestrel
Additional relevant MeSH terms:
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Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Contraceptive Agents, Female
Contraceptive Agents
Reproductive Control Agents
Contraceptives, Oral, Synthetic
Contraceptives, Oral