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Cervical Device Contraception-2 (Nanopaz) (NANOPAZ)

B

Bnai Zion Medical Center

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Healthy

Treatments

Other: Nanopaz contraception device

Study type

Interventional

Funder types

Other

Identifiers

NCT00689494
BnaiZionMC-08-BP-003-CTIL

Details and patient eligibility

About

Measure blood progesterone by using cervical device contraception.

Full 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.

Enrollment

10 estimated patients

Sex

Female

Ages

1 to 2 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 10 healthy women are candidate for hysterectomy

Exclusion criteria

  • Women with neoplastic malignancy disease or thrombophylia

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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